FDA Inspection 1003153 — Thymoorgan Pharmazie Gmbh

Thymoorgan Pharmazie Gmbh — FEI 3002320821

The FDA completed an inspection of Thymoorgan Pharmazie Gmbh on Dec 16, 2016 in Goslar. 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
Dec 16, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Goslar (Germany)

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