FDA Warning Letter — Anigan, Inc.

Case 557163 — FEI 3009666823

The FDA took a Warning Letter action against Anigan, Inc. on July 25, 2018 (San Ramon, CA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Anigan, Inc.
Date
July 25, 2018
Fiscal Year
2018
Product Type
Devices
Center
CDRH
Location
San Ramon, CA (United States)