FDA Inspection 1106642 — Simtra Deutschland GmbH

Simtra Deutschland GmbH — FEI 3002806419

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

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.