FDA Warning Letter — Molteno Ophthalmic Limited

Case 450427 — FEI 3001227772

The FDA took a Warning Letter action against Molteno Ophthalmic Limited on February 27, 2015 (Dunedin, New Zealand). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Molteno Ophthalmic Limited
Date
February 27, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Dunedin (New Zealand)