# Greiner Bio-One North America, Inc. – FDA Inspection, Jan 15, 2010

Source: https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/4e0ea329-1544-4763-8de3-e373e4deb85f
Source feed: FDA_Inspections

> FDA inspection 652912 of Greiner Bio-One North America, Inc., January 15, 2010. Classification: No Action Indicated (NAI). 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 652912
- Company Name: Greiner Bio-One North America, Inc.
- Inspection Date: 2010-01-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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- [FDA Inspection 843981 - 2013-07-24](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/e2c4f6df-eb67-4054-90a5-5c80eb823cc0)

Company: https://www.keypedia.com/companies/greiner-bio-one-north-america-inc/5aa9ea16-ad85-4f85-9b30-efc0ae9b36de

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
