# FDA Inspection 1028572 - OBERON GmbH Fiber Technologies - October 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/oberon-gmbh-fiber-technologies/0b13dc3f-ec9a-4b3c-8e56-f7a93268e069
Source feed: FDA_Inspections

> FDA inspection 1028572 of OBERON GmbH Fiber Technologies, October 13, 2017. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028572
- Company Name: OBERON GmbH Fiber Technologies
- Inspection Date: 2017-10-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1260085 - 2025-02-06](https://www.keypedia.com/records/fda_inspections/oberon-gmbh-fiber-technologies/68c2e9dd-e356-4fa7-82e0-9a7bbc1c8ff0)

Company: https://www.keypedia.com/companies/oberon-gmbh-fiber-technologies/06894df9-c4cf-4f84-8e97-a08ef7d1954b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7