FDA Inspection 729197 — Aerolase Corp.

Aerolase Corp. — FEI 3004374705

The FDA completed an inspection of Aerolase Corp. on Jul 15, 2011 in Tarrytown, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 15, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Tarrytown, NY (United States)

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