# FDA Inspection 926390 - FOTONA D.O.O. - May 14, 2015

Source: https://www.keypedia.com/records/fda_inspections/fotona-doo/434f5fa5-9330-4e04-a4fd-0b657592d800
Source feed: FDA_Inspections

> FDA Inspection 926390 for FOTONA D.O.O. on May 14, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 926390
- Company Name: FOTONA D.O.O.
- Inspection Date: 2015-05-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 926390 - 2015-05-14](https://www.keypedia.com/records/fda_inspections/fotona-doo/ae23311a-db9d-4c6e-9fe6-028f996cc898)

Company: https://www.keypedia.com/companies/fotona-doo/35cd1ada-d86e-4ad4-aef3-132f594b45a3

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