FDA Inspection 779560 — Rottendorf Pharma Gmbh

Rottendorf Pharma Gmbh — FEI 3003732290

The FDA completed an inspection of Rottendorf Pharma Gmbh on Mar 30, 2012 in Ennigerloh. 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
Mar 30, 2012
Fiscal Year
2012
Product Type
Veterinary
Project Area
Pre-Approval Eval. of Animal Drugs and Food Additives
Location
Ennigerloh (Germany)

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