FDA Inspection
Abbott GmbHAbbott GmbH – FDA Inspection, Sep 23, 2010
Record Details
This FDA Inspection record concerns Abbott GmbH, with an inspection on September 23, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Abbott GmbH
- Inspection Date
- September 23, 2010
- Product Type
- Devices
View Company Profile
ID · 286cfcab-dfa1-418b-81d5-cbdf67a45b27
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 684828
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Abbott GmbH
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 23, 2025 | Not classified | Office of Inspections and Investigations | |
| January 17, 2023 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| September 7, 2018 | Not classified | Office of Inspections and Investigations | |
| June 13, 2013 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| February 9, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Abbott GmbH
- FDA Inspection 1275591 - 2025-05-23
- FDA Inspection 1202396 - 2023-01-17
- FDA Inspection 1076420 - 2018-09-07
- FDA Inspection 839385 - 2013-06-13
- FDA Inspection 770439 - 2012-02-09
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