FDA Inspection 1041079 — Precipart Corp

Precipart Corp — FEI 3012227716

The FDA completed an inspection of Precipart Corp on February 9, 2018 in Farmingdale, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 9, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Farmingdale, NY (United States)

Citations

IDCFRDescription
63021 CFR 803.17Lack of Written MDR Procedures