# FDA Inspection 1021970 - Greiner Bio-One North America, Inc. - August 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/2d737c82-b54c-4dca-b236-3358f90507fe
Source feed: FDA_Inspections

> FDA Inspection 1021970 for Greiner Bio-One North America, Inc. on August 17, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021970
- Company Name: Greiner Bio-One North America, Inc.
- Inspection Date: 2017-08-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: 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