FDA Inspection
HIPP medical AGHIPP medical AG – FDA Inspection, Jun 22, 2017
Record Details
This FDA Inspection record concerns HIPP medical AG, with an inspection on June 22, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
View Company Profile
ID · c2411a48-d601-4f52-ac6c-9dd7040dd8f3
Inspection Facts
- Inspection number
- 1015199
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.250(b)Sampling plans
- 21 CFR 820.40(a)Not approved or obsolete document retrieval
Full citation text and observation details available on the Dashboard.
Other FDA inspections of HIPP medical AG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| January 22, 2025 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 11, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for HIPP medical AG
- FDA Inspection 1261902 - 2025-01-22
- FDA Inspection 845588 - 2013-07-11
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.