FDA Warning Letter — Automated Ophthalmics, Inc.

Case 395044 — FEI 3005906810

The FDA took a Warning Letter action against Automated Ophthalmics, Inc. on June 5, 2013 (Elkridge, MD). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Automated Ophthalmics, Inc.
Date
June 5, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Elkridge, MD (United States)