FDA Inspection 1161093 — Simtra Deutschland GmbH

Simtra Deutschland GmbH — FEI 3002806419

The FDA completed an inspection of Simtra Deutschland GmbH on January 29, 2020 in Halle (Westf.). 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
January 29, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Halle (Westf.) (Germany)

Additional Details

Mutual Recognition Agreement (MRA)