FDA Inspection 1068921 — ClearLake-Tech

ClearLake-Tech — FEI 1721293

The FDA completed an inspection of ClearLake-Tech on September 12, 2018 in Clear Lake, SD. 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
September 12, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Clear Lake, SD (United States)