FDA Inspection
GETSCH+HILLER MEDIZINTECHNIK GmbHGETSCH+HILLER MEDIZINTECHNIK GmbH – FDA Inspection, Mar 9, 2017
Record Details
This FDA Inspection record concerns GETSCH+HILLER MEDIZINTECHNIK GmbH, with an inspection on March 9, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- March 9, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 5559cb98-179c-4931-813f-b78a19ab0df6
Inspection Facts
- Inspection number
- 1008330
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of GETSCH+HILLER MEDIZINTECHNIK GmbH
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 21, 2022 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 6, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 28, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for GETSCH+HILLER MEDIZINTECHNIK GmbH
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.