FDA Warning Letter — Clinicon Corp

Case 582801 — FEI 3000719724

The FDA took a Warning Letter action against Clinicon Corp on June 20, 2019 (Oceanside, CA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Clinicon Corp
Date
June 20, 2019
Fiscal Year
2019
Product Type
Devices
Center
CDRH
Location
Oceanside, CA (United States)