FDA Inspection 1263912 — Nordmark Pharma GmbH

Nordmark Pharma GmbH — FEI 3003293533

The FDA completed an inspection of Nordmark Pharma GmbH on February 13, 2025 in Uetersen. 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 13, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Uetersen (Germany)