# FDA Inspection 969398 - Raf-Med - March 31, 2016

Source: https://www.keypedia.com/records/fda_inspections/raf-med/5aa76a37-192c-436b-a137-b0cf903eba25
Source feed: FDA_Inspections

> FDA Inspection 969398 for Raf-Med on March 31, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 969398
- Company Name: Raf-Med
- Inspection Date: 2016-03-31
- 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 969398 - 2016-03-31](https://www.keypedia.com/records/fda_inspections/raf-med/bccc035e-e8cc-4759-b58e-01e7c87df6fe)

Company: https://www.keypedia.com/companies/raf-med/e2cbc3d7-2c11-4794-92f8-b83a06dec523

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