FDA Inspection 1085284 — Pfizer Manufacturing Deutschland GmbH

Pfizer Manufacturing Deutschland GmbH — FEI 3002807097

The FDA completed an inspection of Pfizer Manufacturing Deutschland GmbH on Mar 8, 2019 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
Mar 8, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Freiburg Im Breisgau (Germany)

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