FDA Inspection 1303578 — Rottendorf Pharma Gmbh

Rottendorf Pharma Gmbh — FEI 3003732290

The FDA completed an inspection of Rottendorf Pharma Gmbh on March 14, 2024 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
March 14, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ennigerloh (Germany)

Additional Details

Mutual Recognition Agreement (MRA)