FDA Inspection 972175 — Osteoremedies, LLC
The FDA completed an inspection of Osteoremedies, LLC on Jun 7, 2016 in Memphis, TN. 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
- Jun 7, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Memphis, TN (United States)