FDA Inspection 1268201 — R-Pharm Germany GmbH

R-Pharm Germany GmbH — FEI 3002807165

The FDA completed an inspection of R-Pharm Germany GmbH on February 28, 2023 in Illertissen. 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 28, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Illertissen (Germany)

Additional Details

Mutual Recognition Agreement (MRA)