FDA Inspection 1164258 — Q'apel Medical, Inc.

Q'apel Medical, Inc. — FEI 3015614180

The FDA completed an inspection of Q'apel Medical, Inc. on Mar 8, 2022 in Fremont, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 8, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Fremont, CA (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation
73221 CFR 803.50(a)(2)Individual Report of Malfunction