FDA Inspection
Greiner Bio-One North America, Inc.Greiner Bio-One North America, Inc. – FDA Inspection, Jan 15, 2010
Record Details
This FDA Inspection record concerns Greiner Bio-One North America, Inc., with an inspection on January 15, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 15, 2010
- Product Type
- Devices
View Company Profile
ID · 4e0ea329-1544-4763-8de3-e373e4deb85f
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 652912
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
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 |
| December 13, 2019 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: 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 |
Other documents for Greiner Bio-One North America, Inc.
- FDA Inspection 1222303 - 2023-09-14
- FDA Inspection 1155664 - 2021-10-29
- FDA Inspection 1114241 - 2019-12-13
- FDA Inspection 1021970 - 2017-08-17
- FDA Inspection 843981 - 2013-07-24
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