FDA Warning Letter — Cytophil, Inc.

Case 423633 — FEI 3007225376

The FDA took a Warning Letter action against Cytophil, Inc. on April 1, 2014 (East Troy, WI). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Cytophil, Inc.
Date
April 1, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
East Troy, WI (United States)