FDA Inspection 1013171 — PenCef Pharma GmbH

PenCef Pharma GmbH — FEI 3008654273

The FDA completed an inspection of PenCef Pharma GmbH on May 12, 2017 in Berlin. 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: Veterinary.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 12, 2017
Fiscal Year
2017
Product Type
Veterinary
Project Area
Pre-Approval Eval. of Animal Drugs and Food Additives
Location
Berlin (Germany)

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