FDA Inspection 1053006 — Lincotek Medical
The FDA completed an inspection of Lincotek Medical on Apr 5, 2018 in Logan, UT. 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 5, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Logan, UT (United States)