FDA Inspection 1023316 — Frank Arko
The FDA completed an inspection of Frank Arko on August 14, 2017 in Charlotte, NC. 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
- August 14, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Charlotte, NC (United States)
Additional Details
Clinical Investigator (CI)