FDA Inspection 713161 — Beiersdorf, Inc.

Beiersdorf, Inc. — FEI 1250043

The FDA completed an inspection of Beiersdorf, Inc. on Mar 8, 2011 in Norwalk, CT. 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, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Norwalk, CT (United States)