FDA Inspection 663539 — AES Optics
The FDA completed an inspection of AES Optics on May 20, 2010 in Senatobia, MS. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- May 20, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Senatobia, MS (United States)