# FDA Inspection 1114241 - Greiner Bio-One North America, Inc. - December 13, 2019

Source: https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/49ae4992-a4bf-4cb4-9d7e-60a5ef2b99e7
Source feed: FDA_Inspections

> FDA Inspection 1114241 for Greiner Bio-One North America, Inc. on December 13, 2019. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1114241
- Company Name: Greiner Bio-One North America, Inc.
- Inspection Date: 2019-12-13
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: 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 1222303 - 2023-09-14](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/792ee24d-d397-4690-ad32-0a4e8ae2da1e)
- [FDA Inspection 1155664 - 2021-10-29](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/99c892db-61ca-4cac-87a2-3fefadc27d6b)
- [FDA Inspection 1114241 - 2019-12-13](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/9d28f95a-1841-4858-986f-d6c3d519afb7)
- [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