FDA Inspection 661333 — UltiMed, Inc.
The FDA completed an inspection of UltiMed, Inc. on Apr 29, 2010 in De Smet, SD. 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
- Apr 29, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- De Smet, SD (United States)