FDA Inspection
Greiner Bio-One North America, Inc.Greiner Bio-One North America, Inc. – FDA Inspection, Dec 13, 2019
Record Details
This FDA Inspection record concerns Greiner Bio-One North America, Inc., with an inspection on December 13, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- December 13, 2019
- Product Type
- Devices
View Company Profile
ID · 9d28f95a-1841-4858-986f-d6c3d519afb7
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 1114241
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Enforcement
- Warning Letter
Other FDA inspections of Greiner Bio-One North America, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| September 14, 2023 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 29, 2021 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 17, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 24, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 7, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Greiner Bio-One North America, Inc.
- FDA Inspection 1222303 - 2023-09-14
- FDA Inspection 1155664 - 2021-10-29
- FDA Inspection 1021970 - 2017-08-17
- FDA Inspection 843981 - 2013-07-24
- FDA Inspection 703137 - 2010-12-07
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