# Greiner Bio-One North America, Inc. – FDA Inspection, Oct 29, 2021

Source: https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/99c892db-61ca-4cac-87a2-3fefadc27d6b
Source feed: FDA_Inspections

> FDA inspection 1155664 of Greiner Bio-One North America, Inc., October 29, 2021. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1155664
- Company Name: Greiner Bio-One North America, Inc.
- Inspection Date: 2021-10-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1222303 - 2023-09-14
- [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/2d737c82-b54c-4dca-b236-3358f90507fe)
- [FDA Inspection 843981 - 2013-07-24](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-north-america-inc/e2c4f6df-eb67-4054-90a5-5c80eb823cc0)
- FDA Inspection 703137 - 2010-12-07

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