FDA Inspection
Angiomed GmbH & Co. Medizintechnik KGAngiomed GmbH & Co. Medizintechnik KG – FDA Inspection, Jul 16, 2026
Record Details
This FDA Inspection record concerns Angiomed GmbH & Co. Medizintechnik KG, with an inspection on July 16, 2026, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- July 16, 2026
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · deeeb19a-8fac-4ef5-9954-87ca5f71f804
Inspection Facts
- Inspection number
- 1330386
- 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 |
|---|---|---|---|
| November 15, 2018 | Not classified | Office of Inspections and Investigations | |
| September 27, 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 1106565 - 2018-11-15
- FDA Inspection 1126259 - 2018-09-27
- FDA Inspection 1051603 - 2018-04-12
- FDA Inspection 953098 - 2015-08-20
- FDA Inspection 812973 - 2012-12-13
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.