FDA Inspection 889228 — Fziomed Inc
The FDA completed an inspection of Fziomed Inc on July 24, 2014 in San Luis Obispo, 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
- July 24, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- San Luis Obispo, CA (United States)