FDA Inspection 772259 — ClearLake-Tech

ClearLake-Tech — FEI 1721293

The FDA completed an inspection of ClearLake-Tech on February 29, 2012 in Clear Lake, SD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 29, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Clear Lake, SD (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures