FDA Warning Letter — Molteno Ophthalmic Limited

Case 105145 — FEI 3001227772

The FDA took a Warning Letter action against Molteno Ophthalmic Limited on May 11, 2010 (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
May 11, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Dunedin (New Zealand)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.