FDA Inspection
Siemens Healthcare Diagnostics, Inc.Siemens Healthcare Diagnostics, Inc. – FDA Inspection, Nov 24, 2009
Record Details
This FDA Inspection record concerns Siemens Healthcare Diagnostics, Inc., with an inspection on November 24, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- November 24, 2009
- Product Type
- Devices
View Company Profile
ID · 28ed5b46-4329-40d5-967a-6ca531000e14
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 638744
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
Other FDA inspections of Siemens Healthcare Diagnostics, Inc.
8| Date | Classification | Office | Project area |
|---|---|---|---|
| May 24, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 30, 2022 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 12, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 31, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 19, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Siemens Healthcare Diagnostics, Inc.
- FDA Inspection 1230618 - 2024-05-24
- FDA Inspection 1167476 - 2022-03-30
- FDA Inspection 1141620 - 2021-03-12
- FDA Inspection 1012263 - 2017-05-31
- FDA Inspection 896868 - 2014-09-19
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.