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FDA Inspection 1018322 — Plasti Products Inc

Plasti Products Inc — FEI 1930034

The FDA completed an inspection of Plasti Products Inc on December 9, 2016 in Omaha, NE. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 9, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Omaha, NE (United States)

Facility

Other inspections at this facility

  • 1207693 (NAI Thu May 25 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 815974 (NAI Wed Jan 30 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 816224 (NAI Mon Jan 28 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 706915 (NAI Fri Dec 17 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources