FDA Inspection 1335890 — Pfizer Manufacturing Deutschland GmbH

Pfizer Manufacturing Deutschland GmbH — FEI 3002807097

The FDA completed an inspection of Pfizer Manufacturing Deutschland GmbH on Jul 2, 2025 in Freiburg Im Breisgau. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 2, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Freiburg Im Breisgau (Germany)

Additional Details

Mutual Recognition Agreement (MRA)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.