Animal Legal Defense Fund v. Food & Drug Administration

819 F.3d 1102, 46 Envtl. L. Rep. (Envtl. Law Inst.) 20073, 44 Media L. Rep. (BNA) 2035, 2016 U.S. App. LEXIS 6549, 2016 WL 1399332
CourtCourt of Appeals for the Ninth Circuit
DecidedApril 11, 2016
DocketNo. 13-17131
StatusPublished
Cited by2 cases

This text of 819 F.3d 1102 (Animal Legal Defense Fund v. Food & Drug Administration) is published on Counsel Stack Legal Research, covering Court of Appeals for the Ninth Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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Animal Legal Defense Fund v. Food & Drug Administration, 819 F.3d 1102, 46 Envtl. L. Rep. (Envtl. Law Inst.) 20073, 44 Media L. Rep. (BNA) 2035, 2016 U.S. App. LEXIS 6549, 2016 WL 1399332 (9th Cir. 2016).

Opinions

Opinion by Judge GRABER; per curiam Concurrence.

OPINION

GRABER, Circuit Judge:

Plaintiff Animal Legal Defense Fund filed a Freedom of Information Act (“FOIA”) request with the Food and Drug Administration (“FDA”) regarding egg-production farms in Texas. The FDA released almost 400 pages of documents but redacted data regarding total hen population, number of hen houses, number of floors per house, number of cage rows per house, number of cage tiers per house, and number of birds- per cage for each farm in question.- Plaintiff filed this FOIA action seeking to compel the FDA to release the redacted data. The district court ordered the release of information regarding the number of birds per cage at each farm. But the court held on summary judgment that, under FOIA Exemption 4, the FDA properly withheld the other categories of information because its release was “likely to cause substantial competitive harm.” See 5 U.S.C. § 552(b)(4). • We affirm.

FACTUAL AND PROCEDURAL HISTORY

In late 2011, Plaintiff submitted a FOIA request to the FDA that sought the following:

• All FDA documents since April 26, 2011, relating to egg safety in Texas, egg production in Texas, or egg-production facilities in Texas;
• All FDA communications with Texas state government agencies since April 26, 2011, relating to egg safety, egg production, or egg-production facilities; and
• All communications between the FDA and egg producers in Texas since April 26, 2011.

The FDA released records related to inspections of eleven chicken egg-production facilities; one quail egg-production facility and food manufacturer; one food warehouse; and one food distribution center. But redactions appeared on 277 of the 398 pages that the FDA produced.

[1106]*1106■ Plaintiff filed a complaint for injunctive and declaratory relief under FOIA, 5 U.S.C. § 552, seeking to compel the production of the following information regarding inspected egg-production facilities: total hen population; number of hen houses; number of floors per house; number of cage rows per house; number of cage tiers per house; and number of birds per cage. The FDA moved for summary judgment on the ground that FOIA Exemption 4— which applies to “trade secrets and commercial or financial information obtained from a person and privileged or confidential,” id, -§ 552(b)(4) — protected the redacted data. In support of its motion, the FDA submitted several declarations from experts who stated that releasing the requested information would enable competitors to learn a given egg producer’s production rate, which in turn would allow the competitors to undercut the egg producer’s prices and lure away customers. Plaintiff filed a cross-motion for summary judgment, supported by its own declarations from an economist and a food industry consultant. Those experts attested that releasing the withheld information would not facilitate competitive underbidding.

Plaintiff also asked to suspend briefing of FDA’s summary judgment motion in order to permit discovery directed to whether the information sought was publicly available. The district court denied that request because, among other things, Plaintiff had not shown that the discovery it 'sought “is essential to litigating the motion for summary judgment.”

After briefing and oral argument, the district court granted in part and denied in part both parties’ summary judgment motions. The district court held that the FDA had fallen short of showing how releasing the number of birds per cage would “threaten any competitive harm” and ordered disclosure of that information. But the court concluded that the FDA had established that the release of the other five categories of redacted information— total hen population, number of hen houses, number of floors per house, number of cage rows per house, and number of cage tiers per house — was likely to result in substantial competitive harm due to underbidding.

Plaintiff timely appeals the court’s grant of summary judgment in favor of the FDA on the redaction of those five categories of information, as well as the denial of third-party discovery.

STANDARDS OF REVIEW

“Our review of a grant of summary judgment in a FOIA case ... is slightly different than for other types of cases....” Yonemoto v. Dep’t of Veterans Affairs, 686 F.3d 681, 688 (9th Cir.2012). We first determine, de novo, whether an adequate factual basis supports the district court’s decision. Id. “Whether a particular set of documents gives the court an adequate ’ factual basis for its decision is a question of law that the court reviews de novo.’’ Lion Raisins, Inc. v. U.S. Dep’t of Agric, 354 F.3d 1072, 1078 (9th Cir.2004). If no adequate. factual basis exists, the case must be remanded for further- development of the record. Yonemoto, 686 F.3d at 688.

If such a factual basis exists, we next treat the judgment as “if it were a bench trial,” so that “the district court’s conclusions of fact are reviewed for clear error.” Id. (internal quotation marks omitted). On the other hand, “legal rulings, including [the district court’s] decision that a particular exemption applies, are reviewed de novo.” Id. As we noted in Lion Raisins, whether withheld information could be used by a food producer to undercut competitors is a determination that is “grounded in ... findings of fact.” [1107]*1107354 F.3d at 1078. Therefore, if we determine that the district court had an adequate factual basis for reaching, its decision, we must review for clear error the district court’s conclusion that releasing the redacted information likely would cause substantial competitive harm. Id.

We review for abuse of discretion a district court’s denial of discovery before ruling on summary judgment. U.S. Cellular Inv. Co. of L.A., Inc. v. GTE Mobilnet, Inc., 281 F.3d 929, 934 (9th Cir.2002).

DISCUSSION

A. Disclosure Under FOIA

“Disclosure, not secrecy, is the dominant objective of FOIA.” Shannahan v. IRS, 672 F.3d 1142, 1148 (9th Cir.2012) (internal quotation marks • and brackets omitted). “We construe narrowly FOIA’s nine exemptions.” Id. The FDA relies on Exemption 4, 5 U.S.C. § 552(b)(4); “which is available to prevent disclosure of (1) commercial and financial ■ information, (2) obtained from a person or by the government, (3) that is privileged or confidential.” 1 GC Micro Corp. v. Def. Logistics Agency, 33 F.3d 1109, 1112 (9th Cir.1994). Commercial information qualifies as “confidential” when disclosure is “likely .... to cause substantial harm to the competitive position of the person from whom the information was obtained.” Id. 1112-13.(citing Nat’l Parks & Conservation Ass’n v. Morton,

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819 F.3d 1102, 46 Envtl. L. Rep. (Envtl. Law Inst.) 20073, 44 Media L. Rep. (BNA) 2035, 2016 U.S. App. LEXIS 6549, 2016 WL 1399332, Counsel Stack Legal Research, https://law.counselstack.com/opinion/animal-legal-defense-fund-v-food-drug-administration-ca9-2016.