FDA Inspection 999722 — Korchek Technologies LLC

Korchek Technologies LLC — FEI 3004587266

The FDA completed an inspection of Korchek Technologies LLC on February 7, 2017 in Trumbull, CT. 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
February 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Trumbull, CT (United States)