# FDA Inspection 1222303 - Greiner Bio-One North America, Inc. - September 14, 2023

Source: https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/792ee24d-d397-4690-ad32-0a4e8ae2da1e
Source feed: FDA_Inspections

> FDA Inspection 1222303 for Greiner Bio-One North America, Inc. on September 14, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1222303
- Company Name: Greiner Bio-One North America, Inc.
- Inspection Date: 2023-09-14
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1222303 - 2023-09-14](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/70df1992-fe14-47c9-9d60-af1f9ddac385)
- [FDA Inspection 1155664 - 2021-10-29](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/99c892db-61ca-4cac-87a2-3fefadc27d6b)
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- [FDA Inspection 1021970 - 2017-08-17](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/2a521195-52f0-43d5-952c-c067e9576808)

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