FDA Inspection 930102 — Herman H. Schroe, MD
The FDA completed an inspection of Herman H. Schroe, MD on April 24, 2015 in Genk. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- April 24, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Genk (Belgium)
Additional Details
Clinical Investigator (CI)