FDA Inspection 761354 — Serumwerk Bernburg AG

Serumwerk Bernburg AG — FEI 3003903447

The FDA completed an inspection of Serumwerk Bernburg AG on Dec 1, 2011 in Bernburg (Saale). 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
Dec 1, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bernburg (Saale) (Germany)