Greiner Bio-One North America, Inc.

Form 483

Monroe, North Carolina, United StatesFEI 3001451379Issued August 17, 2017

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3001451379.

Observations6

Issue DateAugust 17, 2017

Status1 Related Warning Letter

Related Inspections7

Establishment Details

Firm: Greiner Bio-One North America, Inc.
Location: Monroe, North Carolina, United States
FEI Number: 3001451379
Product Type: Devices
Issue Date: August 17, 2017
Country: United States

Inspection History, 2010 to 2023

NAI3

VAI3

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Greiner Bio-One North America, Inc. FDA Form 483, Monroe, North Carolina, August 17, 2017