FDA Inspection 581953 — Dunteman MS, Dr Edwin
The FDA completed an inspection of Dunteman MS, Dr Edwin on May 1, 2009 in Creve Coeur, MO. 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
- May 1, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Creve Coeur, MO (United States)
Additional Details
Clinical Investigator (CI)