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FDA Inspection
•Wyeth Pharmaceutical Division of Wyeth Holdings LLC•November 18, 2011

Wyeth Pharmaceutical Division of Wyeth Holdings LLC – FDA Inspection, Nov 18, 2011

Record Details

This FDA Inspection record concerns Wyeth Pharmaceutical Division of Wyeth Holdings LLC, with an inspection on November 18, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Wyeth Pharmaceutical Division of Wyeth Holdings LLC
Inspection Date
November 18, 2011
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · d2def70c-934c-43e2-b20f-8c5d91d8edbb

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
758809
FDA center
Biologics
Project area
Vaccines and Allergenic Products

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
October 17, 2024Not classifiedAtlanta District Office
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
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 1252280 - 2024-10-17
  • FDA Inspection 1234989 - 2023-11-10
  • FDA Inspection 1192736 - 2022-11-18
  • FDA Inspection 1121288 - 2019-11-26

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