# FDA Inspection 983863 - SGM D.O.O. - August 25, 2016

Source: https://www.keypedia.com/records/fda_inspections/sgm-doo/873e8fa7-e587-4a97-80e2-fbcfb929316a
Source feed: FDA_Inspections

> FDA Inspection 983863 for SGM D.O.O. on August 25, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 983863
- Company Name: SGM D.O.O.
- Inspection Date: 2016-08-25
- 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 983863 - 2016-08-25](https://www.keypedia.com/records/fda_inspections/sgm-doo/750ecc6c-58b2-498f-883a-7622625c0d25)

Company: https://www.keypedia.com/companies/sgm-doo/406b5e1f-06eb-46e6-8d18-c594441140ac

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