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FDA Inspection 703137 — 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 7, 2010 in Monroe, NC. 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
December 7, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Monroe, NC (United States)

Facility

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Recent compliance actions

FDA data resources