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FDA Inspection
•Wyeth Pharmaceutical Division of Wyeth Holdings LLC•October 17, 2024

Wyeth Pharmaceutical Division of Wyeth Holdings LLC – FDA Inspection, Oct 17, 2024

Record Details

This FDA Inspection record concerns Wyeth Pharmaceutical Division of Wyeth Holdings LLC, with an inspection on October 17, 2024, issued by the Atlanta District Office, covering biologics.

Company
Wyeth Pharmaceutical Division of Wyeth Holdings LLC
Inspection Date
October 17, 2024
Product Type
Biologics
Office
Atlanta District Office
People
  • Burnell M. Henry (FDA Associated Person)
  • Unnee Ranjan (FDA Associated Person)
View Company Profile

ID · 8edcf3d1-8ada-4d4b-a7da-57756242fc94

Inspection Facts

Inspection number
1252280
FDA center
Biologics
Outcome
Form 483 issued, view the record

Other FDA inspections of Wyeth Pharmaceutical Division of Wyeth Holdings LLC

10
DateClassificationOfficeProject area
April 23, 2026Not classifiedAtlanta District OfficeHuman Cellular, Tissue, and Gene Therapies
November 10, 2023Not classifiedAtlanta District Office
November 18, 2022VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
November 26, 2019VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
April 19, 2018VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
View all 10 other inspections on the company page
Other documents for Wyeth Pharmaceutical Division of Wyeth Holdings LLC
  • FDA Inspection 1305396 - 2026-04-23
  • FDA Inspection 1234989 - 2023-11-10
  • FDA Inspection 1192736 - 2022-11-18
  • FDA Inspection 1121288 - 2019-11-26
  • FDA Inspection 1051716 - 2018-04-19

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