FDA Warning Letter — Ambu Inc.

Case 661617 — FEI 1121788

The FDA took a Warning Letter action against Ambu Inc. on Aug 16, 2023 (Columbia, MD). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Ambu Inc.
Date
Aug 16, 2023
Fiscal Year
2023
Product Type
Devices
Center
CDRH
Location
Columbia, MD (United States)

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