# FDA Inspection 1026647 - Medifix, Inc. - August 08, 2017

Source: https://www.keypedia.com/records/fda_inspections/medifix-inc/3eb6b62b-c08f-4bed-a039-9c257dd02f98
Source feed: FDA_Inspections

> FDA Inspection 1026647 for Medifix, Inc. on August 08, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026647
- Company Name: Medifix, Inc.
- Inspection Date: 2017-08-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 822164 - 2013-03-18](https://www.keypedia.com/records/fda_inspections/medifix-inc/bb089d44-e415-47cb-b608-ac096d2c7c5a)
- [FDA Inspection 822164 - 2013-03-18](https://www.keypedia.com/records/fda_inspections/medifix-inc/b05fc687-6b41-4975-9607-8b13ea61b34e)
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Company: https://www.keypedia.com/companies/medifix-inc/a82e7526-4444-42e3-9e58-8b66ecee1439

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