FDA Inspection 1251210 — Beiersdorf AG

Beiersdorf AG — FEI 3002806448

The FDA completed an inspection of Beiersdorf AG on December 9, 2021 in Hamburg. 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
December 9, 2021
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hamburg (Germany)

Additional Details

Mutual Recognition Agreement (MRA)