FDA Inspection 1115028 — Phamedica Inc.

Phamedica Inc. — FEI 3011848308

The FDA completed an inspection of Phamedica Inc. on January 10, 2020 in Plainview, 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
January 10, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Plainview, NY (United States)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation
63021 CFR 803.17Lack of Written MDR Procedures