FDA Inspection 1106642 — Simtra Deutschland GmbH

Simtra Deutschland GmbH — FEI 3002806419

The FDA completed an inspection of Simtra Deutschland GmbH on September 3, 2019 in Halle (Westf.). The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 3, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Halle (Westf.) (Germany)