FDA Inspection
Admedes GmbHAdmedes GmbH – FDA Inspection, Dec 11, 2014
Record Details
This FDA Inspection record concerns Admedes GmbH, with an inspection on December 11, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Admedes GmbH
- Inspection Date
- December 11, 2014
- Product Type
- Devices
View Company Profile
ID · 03f91ba1-7d36-42da-bf28-7588ff8238fe
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 908900
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 820.70(a)Production processes
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Admedes GmbH
4| Date | Classification | Office | Project area |
|---|---|---|---|
| June 15, 2023 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 7, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 2, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 25, 2009 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Admedes GmbH
- FDA Inspection 1210941 - 2023-06-15
- FDA Inspection 1078412 - 2018-12-07
- FDA Inspection 711358 - 2011-03-02
- FDA Inspection 596171 - 2009-06-25
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.