FDA Inspection 815296 — AcuFocus, Inc.

AcuFocus, Inc. — FEI 3008401069

The FDA completed an inspection of AcuFocus, Inc. on Jan 18, 2013 in Irvine, CA. 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
Jan 18, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)

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