FDA Inspection 1288424 — Conair LLC

Conair LLC — FEI 1000121041

The FDA completed an inspection of Conair LLC on October 22, 2025 in Stamford, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 22, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Stamford, CT (United States)

Citations

IDCFRDescription
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures