FDA Inspection 663539 — AES Optics

AES Optics — FEI 3003790338

The FDA completed an inspection of AES Optics on May 20, 2010 in Senatobia, MS. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
May 20, 2010
Fiscal Year
2010
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.