FDA Inspection 724204 — AES Optics

AES Optics — FEI 3003790338

The FDA completed an inspection of AES Optics on Apr 11, 2011 in Senatobia, MS. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 11, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Senatobia, MS (United States)

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