FDA Inspection
Angiomed GmbH & Co. Medizintechnik KGAngiomed GmbH & Co. Medizintechnik KG – FDA Inspection, Sep 27, 2018
Record Details
This FDA Inspection record concerns Angiomed GmbH & Co. Medizintechnik KG, with an inspection on September 27, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- September 27, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · f325dbfc-2b13-4f5f-9cf0-25aa20262cd1
Inspection Facts
- Inspection number
- 1126259
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Angiomed GmbH & Co. Medizintechnik KG
6| Date | Classification | Office | Project area |
|---|---|---|---|
| July 16, 2026 | Not classified | Office of Inspections and Investigations | |
| November 15, 2018 | Not classified | Office of Inspections and Investigations | |
| April 12, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 20, 2015 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| December 13, 2012 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Angiomed GmbH & Co. Medizintechnik KG
- FDA Inspection 1330386 - 2026-07-16
- FDA Inspection 1106565 - 2018-11-15
- FDA Inspection 1051603 - 2018-04-12
- FDA Inspection 953098 - 2015-08-20
- FDA Inspection 812973 - 2012-12-13
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