FDA Inspection 1039792 — Conair LLC

Conair LLC — FEI 1000121041

The FDA completed an inspection of Conair LLC on February 1, 2018 in Stamford, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 1, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Stamford, CT (United States)

Citations

IDCFRDescription
260421 CFR 820.30(e)Design review - Lack of or inadequate procedures
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures