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
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ID · 0b13dc3f-ec9a-4b3c-8e56-f7a93268e069
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1028572
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: 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 |
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