FDA Warning Letter — Mooncup LTD

Case 495541 — FEI 3009117944

The FDA took a Warning Letter action against Mooncup LTD on May 27, 2016 (Brighton, United Kingdom). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Mooncup LTD
Date
May 27, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Brighton (United Kingdom)