FDA Inspection 836648 — Diacor, Inc
The FDA completed an inspection of Diacor, Inc on June 19, 2013 in West Valley City, UT. 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
- June 19, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- West Valley City, UT (United States)