# FDA Inspection 843981 - Greiner Bio-One North America, Inc. - July 24, 2013

Source: https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/e2c4f6df-eb67-4054-90a5-5c80eb823cc0
Source feed: FDA_Inspections

> FDA Inspection 843981 for Greiner Bio-One North America, Inc. on July 24, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 843981
- Company Name: Greiner Bio-One North America, Inc.
- Inspection Date: 2013-07-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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