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FDA Inspection 583525 — Pentax of America Inc

Pentax of America Inc — FEI 1000080301

The FDA completed an inspection of Pentax of America Inc on May 18, 2009 in Montvale, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 18, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Montvale, NJ (United States)

Facility

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  • 921077 (OAI Thu Apr 02 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 906155 (VAI Wed Dec 17 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
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Recent compliance actions

FDA data resources