FDA Inspection 1040206 — Lincotek Medical LLC.
The FDA completed an inspection of Lincotek Medical LLC. on Jan 12, 2018 in Vandalia, OH. 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
- Jan 12, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Vandalia, OH (United States)