# FDA Inspection 1031662 - Meluna - November 09, 2017

Source: https://www.keypedia.com/records/fda_inspections/meluna/47bc9eae-cb28-41a7-8bd9-c471263f4522
Source feed: FDA_Inspections

> FDA Inspection 1031662 for Meluna on November 09, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031662
- Company Name: Meluna
- Inspection Date: 2017-11-09
- 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 1031662 - 2017-11-09](https://www.keypedia.com/records/fda_inspections/meluna/0b8700fc-5d65-4f96-a37e-defd5aa93174)

Company: https://www.keypedia.com/companies/meluna/02903460-9ca4-4868-b754-1740e04dffdb

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