FDA Inspection 675484 — Prowess, Inc.
The FDA completed an inspection of Prowess, Inc. on August 11, 2010 in Concord, CA. 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 11, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Concord, CA (United States)