FDA Warning Letter — Digitimer Ltd.

Case 479856 — FEI 3003631667

The FDA took a Warning Letter action against Digitimer Ltd. on Oct 19, 2015 (Welwyn Garden City, United Kingdom). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Digitimer Ltd.
Date
Oct 19, 2015
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Welwyn Garden City (United Kingdom)