FDA Warning Letter — Cellestis Inc

Case 458031 — FEI 3003964343

The FDA took a Warning Letter action against Cellestis Inc on August 26, 2015 (Santa Clarita, CA). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Cellestis Inc
Date
August 26, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Santa Clarita, CA (United States)