FDA Inspection 1122506 — Lincotek Medical

Lincotek Medical — FEI 3008421730

The FDA completed an inspection of Lincotek Medical on March 12, 2020 in Bartlett, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 12, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Bartlett, TN (United States)