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FDA Inspection 904825 — Pinook USA, LLC

Pinook USA, LLC — FEI 3008113239

The FDA completed an inspection of Pinook USA, LLC on December 2, 2014 in Orlando, FL. 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
December 2, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Orlando, FL (United States)

Facility

Other inspections at this facility

  • 927022 (OAI Wed May 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 821133 (OAI Fri Mar 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 769446 (OAI Fri Feb 24 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources