FDA Warning Letter — Magnolia Medical Technologies, Inc.

Case 617922 — FEI 3009976527

The FDA took a Warning Letter action against Magnolia Medical Technologies, Inc. on Sep 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
Sep 17, 2021
Fiscal Year
2021
Product Type
Devices
Center
CDRH
Location
Seattle, WA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.