FDA Warning Letter — DSAART LLC

Case 618157 — FEI 3003897287

The FDA took a Warning Letter action against DSAART LLC on November 24, 2021 (Carson City, NV). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
DSAART LLC
Date
November 24, 2021
Fiscal Year
2022
Product Type
Devices
Center
CDRH
Location
Carson City, NV (United States)