FDA Inspection 729197 — Aerolase Corp.

Aerolase Corp. — FEI 3004374705

The FDA completed an inspection of Aerolase Corp. on July 15, 2011 in Tarrytown, NY. 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
July 15, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Tarrytown, NY (United States)