FDA Inspection 1009131 — Oscor Inc.
The FDA completed an inspection of Oscor Inc. on March 23, 2017 in Palm Harbor, FL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- March 23, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Palm Harbor, FL (United States)