FDA Inspection 910476 — PharmaZell GmbH

PharmaZell GmbH — FEI 3003725792

The FDA completed an inspection of PharmaZell GmbH on December 12, 2014 in Raubling. 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 12, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Raubling (Germany)