FDA Inspection 1052182 — Osteomedix Inc
The FDA completed an inspection of Osteomedix Inc on Apr 27, 2018 in Grayslake, IL. 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 27, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Grayslake, IL (United States)