# Greiner Bio-One GmbH – FDA Inspection, Dec 21, 2023

Source: https://www.keypedia.com/records/fda_inspections/greiner-bio-one-gmbh/d1a2a428-2799-48e1-a020-885b852c03b6
Source feed: FDA_Inspections

> FDA inspection 1226348 of Greiner Bio-One GmbH, December 21, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1226348
- Company Name: Greiner Bio-One GmbH
- Inspection Date: 2023-12-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1069716 - 2018-10-25](https://www.keypedia.com/records/fda_inspections/greiner-bio-one-gmbh/c998d201-79b4-4c1e-916b-2e6be589cec0)

## Related Officers

- [Investigator](https://www.keypedia.com/people/david-m-wilkinson/5e81ba03-7602-46d6-b675-26efc77d28db)

Company: https://www.keypedia.com/companies/greiner-bio-one-gmbh/3eeba95c-99e8-4ab8-8478-7dbc994a4970

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7