FDA Warning Letter — Q'apel Medical, Inc.

Case 699244 — FEI 3015614180

The FDA took a Warning Letter action against Q'apel Medical, Inc. on Feb 5, 2025 (Fremont, CA). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Q'apel Medical, Inc.
Date
Feb 5, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
Fremont, CA (United States)