FDA Warning Letter — Magnolia Medical Technologies, Inc.

Case 617922 — FEI 3009976527

The FDA took a Warning Letter action against Magnolia Medical Technologies, Inc. on September 17, 2021 (Seattle, WA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Magnolia Medical Technologies, Inc.
Date
September 17, 2021
Fiscal Year
2021
Product Type
Devices
Center
CDRH
Location
Seattle, WA (United States)