FDA Inspection 598379 — Protek Medical Products Inc
The FDA completed an inspection of Protek Medical Products Inc on July 21, 2009 in Coralville, IA. 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
- July 21, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Coralville, IA (United States)