FDA Inspection 1268201 — R-Pharm Germany GmbH

R-Pharm Germany GmbH — FEI 3002807165

The FDA completed an inspection of R-Pharm Germany GmbH on Feb 28, 2023 in Illertissen. 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: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 28, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Illertissen (Germany)

Additional details

Mutual Recognition Agreement (MRA)

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