Phan v. Hhs

Court of Appeals for the Federal Circuit·Decided November 1, 2023·No. 22-1749·Unpublished

Opinion

NOTE: This disposition is nonprecedential.

United States Court of Appeals for the Federal Circuit

VINH PHAN,

Petitioner

v.

DEPARTMENT OF HEALTH AND HUMAN SERVICES, Respondent

2022-1749

Petition for review of the Merit Systems Protection Board in No. DE-1221-21-0252-W-1.

Decided: November 1, 2023

VINH PHAN, Shawnee, KS, pro se.

LAURA OFFENBACHER ARADI, Commercial Litigation Branch, Civil Division, United States Department of Justice , Washington, DC, for respondent. Also represented by REGINALD THOMAS BLADES, JR., BRIAN M. BOYNTON, PATRICIA M. MCCARTHY.

Before NEWMAN, LOURIE, and PROST, Circuit Judges.

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Opinion for the court filed PER CURIAM.

Dissenting opinion filed by Circuit Judge NEWMAN.

PER CURIAM.

Vinh Phan appeals from a decision of the Merit Systems Protection Board (“Board”) denying a request for relief in an Individual Right of Action appeal that asserted retaliatory agency action for alleged whistleblowing activity . Phan v. Dep’t of Health & Hum. Servs., 2022 WL 509255 (M.S.P.B. Feb. 14, 2022) (“Decision”), R.A. 6–33. 1 For the following reasons, we affirm in part and vacate and remand in part.

BACKGROUND

In 2003, Phan began working as a chemist in the Kansas City District Laboratory (“KCL”) of the Food and Drug Administration (“FDA”), a division of the Department of Health and Human Services. R.A. 45. Over the years, Phan rose to a GS-1320-12 Step 8 position. Id. In March 2020, Phan applied for a promotion to a GS-13 Team Lead position after learning that four such positions had become available. Id. In July 2020, KCL announced the four individuals to be promoted. Id. Phan was not one of them. Id.

In a complaint to the Office of Special Counsel (“OSC”), Phan asserted that KCL retaliated against him for whistleblowing activity in violation of 5 U.S.C. § 2302(b)(8). R.A. 45, 49−52. The complaint alleges whistleblowing activity relating to a letter, sent by another chemist at KCL, Linwood Daughtry II, to a U.S. Senator. Id. at 45−46. The half-page letter listed “concerns of [Daughtry] as well as coworkers that have yet to be addressed by upper management .” Id. at 43. In particular, it listed:

1 “R.A.” refers to the appendix filed with Respondent ’s brief.

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• Agency’s Diversity and EEO Policy violation • Hiring and Promotion of Qualified Personnel • Awards and Performance Management Appraisal Program

• Mismanagement of taxpayer’s monies R.A. 43. The letter included no further details on those four areas of alleged concern. Phan and six other coworkers cosigned Daughtry’s letter, id. at 43−44, which was eventually forwarded to various supervisors at KCL as well as upper management at the FDA.

The FDA began an investigation into KCL employment practices in 2019 following the letter. As part of that investigation , Phan alleges the signatories of the letter met face-to-face with FDA investigators on March 7, 2019. Appellant ’s Br. at 3; see P.A. 42–44. 2 Phan sent an email on March 8, 2019, to FDA investigators and the FDA Associate Commissioner of Regulatory Affairs. P.A. 46–47. On July 17, 2019, Phan provided an affidavit. P.A. 49–54.

In his complaint to OSC, Phan asserted that the “only explanation for [his] non-selection [for the Team Lead position ] is that the interviewers colluded to downgrade [his] interviewing score and ranking . . . [to] eliminate [him] from selection in retaliation for whistle blowing activities.” R.A. 51. In addition to being denied the Team Lead promotion , Phan alleged further retaliation in the form of a proposal by KCL management to transfer him to a new research group, as well as a denial of a Quality Step Increase . Id. at 47−49. Notably, Phan was never transferred, as he asked not to be, and that preference to not be transferred was honored. Decision at 13 (noting that Phan’s supervisor purportedly offered Phan the opportunity to switch research groups because the supervisor believed

2 “P.A.” refers to the appendix filed with Petitioner’s brief.

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that Phan “was the most capable person under [his] supervision ”). Similarly, although Phan did not receive a Quality Step Increase, he was awarded a cash bonus and timeoff award in exchange for an outstanding work performance . Id. at 14.

Phan then filed an Individual Right of Action appeal under the Whistleblower Protection Act as amended by the Whistleblower Protection Enhancement Act. Decision at 1−2. In her initial decision, the administrative judge, without a hearing, found that Phan did not meet his burden of showing that he made protected disclosures or engaged in protected activity. Id. at 17−19. That decision became the Board’s final decision on March 21, 2022. Id. at 20; see 5 C.F.R. § 1201.113. Phan appealed. We have jurisdiction under 28 U.S.C. § 1295(a)(9).

DISCUSSION

Phan contends that the Board erred in holding that he failed to establish that he engaged in a protected disclosure under 5 U.S.C. § 2302(b)(8) by co-signing Daughtry’s letter. The Board concluded, and we agree, that the letter did not constitute a protected disclosure because it only stated general concerns rather than substantive details. “A party cannot establish jurisdiction through general assertions, but must provide substantive details.” Young v. Merit Sys. Prot. Bd., 961 F.3d 1323, 1328 (Fed. Cir. 2020); Johnston v. Merit Sys. Prot. Bd., 518 F.3d 905, 910 (Fed. Cir. 2008) (“[V]ague, conclusory[,] or facially insufficient allegations of government wrongdoing . . . fail to provide an adequate jurisdictional predicate under the [Whistleblower Protection Act].”).

Phan next contends that the Board “failed to take into account the fact that signatories discussed the bullet points of the letter (and more) in detail in a face-to-face meeting with” FDA investigators. Appellant’s Br. at 3. He further contends that an email sent to two FDA investigators as well as the FDA Associate Commissioner of Regulatory

PHAN v. HHS 5

Affairs was a “detail[ed] disclosure.” Id. And he makes the same assertion regarding an affidavit he submitted during that internal investigation. Id.

The Board analyzed Phan’s participation in the FDA’s investigation under 5 U.S.C. § 2302(b)(9). Protected activity under § 2302(b)(9) includes:

(A) the exercise of any appeal, complaint, or grievance right granted by any law, rule, or regulation—

(i) with regard to remedying a violation of paragraph (8); or (ii) other than with regard to remedying a violation of paragraph (8);

(B) testifying for or otherwise lawfully assisting any individual in the exercise of any right referred to in subparagraph (A)(i) or (ii); (C) cooperating with or disclosing information to the Inspector General (or any other component responsible for internal investigation or review) of an agency, or the Special Counsel, in accordance with applicable provisions of law; or (D) refusing to obey an order that would require the individual to violate a law, rule, or regulation[.]

5 U.S.C. § 2302(b)(9) (emphasis added).

A previous version of § 2302(b)(9)(C) defined its protected activity only as “cooperating with or disclosing information to the Inspector General of an agency, or the Special Counsel, in accordance with applicable provisions of law.” 5 U.S.C. § 2302(b)(9)(C) (2016). In 2017, however, Congress added the “or any other component responsible for internal investigation or review” parenthetical (emphasized above) in the National Defense Authorization Act for Fiscal Year 2018 (“NDAA”), Pub. L. No. 115-91, sec. 1097(c)(1)(A), 131 Stat. 1283, 1618.

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