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 Dec 13, 2019 in Monroe, NC. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Dec 13, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Monroe, NC (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.