FDA Inspection 1242777 — Propper Mfg Co Inc

Propper Mfg Co Inc — FEI 2410251

The FDA completed an inspection of Propper Mfg Co Inc on June 13, 2024 in Long Island City, NY. 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
June 13, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Long Island City, NY (United States)

Citations

IDCFRDescription
368321 CFR 820.70(g)Equipment Installation, Placement, Specified Requirements
63021 CFR 803.17Lack of Written MDR Procedures