FDA Inspection
OBERON GmbH Fiber TechnologiesFDA Inspection 1028572 - OBERON GmbH Fiber Technologies - October 13, 2017
Record Details
This FDA Inspection record concerns OBERON GmbH Fiber Technologies, with an inspection on October 13, 2017, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- October 13, 2017
- Product Type
- Devices
View Company Profile
ID · 408e6623-0fbb-4598-880d-0f74363906ba
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1028572
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of OBERON GmbH Fiber Technologies
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2025 | Not classified | Office of Inspections and Investigations | Compliance: Medical Devices |
Other documents for OBERON GmbH Fiber Technologies
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.