FDA Inspection 571620 — Adalberto Sperb Rubin, M.D.
The FDA completed an inspection of Adalberto Sperb Rubin, M.D. on Mar 5, 2009 in Porto Alegre. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Mar 5, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Porto Alegre (Brazil)
Additional Details
Clinical Investigator (CI)