FDA Inspection
Geistlich Pharma AGGeistlich Pharma AG – FDA Inspection, Jun 22, 2017
Record Details
This FDA Inspection record concerns Geistlich Pharma AG, with an inspection on June 22, 2017, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Geistlich Pharma AG
- Inspection Date
- June 22, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 5b208e26-3c31-4029-8cfc-6496e68d8f0d
Inspection Facts
- Inspection number
- 1031529
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Geistlich Pharma AG
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 12, 2009 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Geistlich Pharma AG
- FDA Inspection 563924 - 2009-02-12
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.