FDA Warning Letter — Aquavit Life Sciences, Inc.

Case 607150 — FEI 3010704000

The FDA took a Warning Letter action against Aquavit Life Sciences, Inc. on Jun 17, 2021 (Las Vegas, NV). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Aquavit Life Sciences, Inc.
Date
Jun 17, 2021
Fiscal Year
2021
Product Type
Devices
Center
CDRH
Location
Las Vegas, NV (United States)

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