FDA Inspection 1312340 — Dr. Astrid Breitschaft

Dr. Astrid Breitschaft — FEI 3043274325

The FDA completed an inspection of Dr. Astrid Breitschaft on Mar 27, 2026 in Berlin. 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
Mar 27, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Berlin (Germany)

Additional details

Clinical BA/BE

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