FDA Inspection 1083771 — Rottendorf Pharma Gmbh

Rottendorf Pharma Gmbh — FEI 3003732290

The FDA completed an inspection of Rottendorf Pharma Gmbh on February 21, 2019 in Ennigerloh. 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
February 21, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ennigerloh (Germany)