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FDA Inspection 1085284 — Pfizer Manufacturing Deutschland GmbH

Pfizer Manufacturing Deutschland GmbH — FEI 3002807097

The FDA completed an inspection of Pfizer Manufacturing Deutschland GmbH on March 8, 2019 in Freiburg Im Breisgau. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 8, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Freiburg Im Breisgau (Germany)

Facility

Other inspections at this facility

  • 1222873 (VAI Thu May 11 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1021100 (NAI Tue Jun 27 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 966853 (NAI Fri Mar 04 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 875506 (VAI Thu Apr 03 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 788967 (VAI Fri Jun 15 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources