FDA Warning Letter — AES Optics

Case 117612 — FEI 3003790338

The FDA took a Warning Letter action against AES Optics on November 18, 2010 (Senatobia, MS). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
AES Optics
Date
November 18, 2010
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Senatobia, MS (United States)