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FDA Inspection 1114241 — Greiner Bio-One North America, Inc.

Greiner Bio-One North America, Inc. — FEI 3001451379

The FDA completed an inspection of Greiner Bio-One North America, Inc. on December 13, 2019 in Monroe, NC. 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 13, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Monroe, NC (United States)

Facility

Other inspections at this facility

  • 1222303 (NAI Thu Sep 14 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1155664 (VAI Fri Oct 29 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1021970 (NAI Thu Aug 17 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 843981 (VAI Wed Jul 24 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 703137 (NAI Tue Dec 07 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources