# FDA Inspection 1208833 - NEOSS AB - June 27, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/neoss-ab/dd592a8f-88a0-4ed3-9ff4-5f3014e0520c
Source feed: FDA_Inspections

> FDA Inspection 1208833 for NEOSS AB on June 27, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1208833
- Company Name: NEOSS AB
- Inspection Date: 2023-06-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1208833 - 2023-06-27](https://www.globalkeysolutions.net/records/fda_inspections/neoss-ab/2072a512-6e59-4ed7-ac8b-a9777440f108)

Company: https://www.globalkeysolutions.net/companies/neoss-ab/369d6951-1b66-446a-a302-21995af59e37

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