# FDA Inspection 995999 - MEGIN OY - October 27, 2016

Source: https://www.keypedia.com/records/fda_inspections/megin-oy/6aec55bb-5018-4701-82f8-c45385950fcc
Source feed: FDA_Inspections

> FDA Inspection 995999 for MEGIN OY on October 27, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 995999
- Company Name: MEGIN OY
- Inspection Date: 2016-10-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 995999 - 2016-10-27](https://www.keypedia.com/records/fda_inspections/megin-oy/2c0ea010-55d0-4893-878b-09e8c3251778)
- [FDA Inspection 794673 - 2012-07-19](https://www.keypedia.com/records/fda_inspections/megin-oy/4927e8f3-5236-4d66-9db2-34c124dc8998)

Company: https://www.keypedia.com/companies/megin-oy/87686927-a071-45c1-9ec4-50845f47a118

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