# FDA Inspection 1110192 - Fivos, Inc. - November 07, 2019

Source: https://www.keypedia.com/records/fda_inspections/fivos-inc/4b64ccd2-be51-4a4f-b30b-94a1bb26c37e
Source feed: FDA_Inspections

> FDA Inspection 1110192 for Fivos, Inc. on November 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1110192
- Company Name: Fivos, Inc.
- Inspection Date: 2019-11-07
- 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 1110192 - 2019-11-07](https://www.keypedia.com/records/fda_inspections/fivos-inc/6fc9b4da-d55e-416c-93c5-b19b437c83fe)
- [FDA Inspection 997578 - 2017-01-05](https://www.keypedia.com/records/fda_inspections/fivos-inc/1395067d-42d8-4a10-ae8f-192ad4662065)
- [FDA Inspection 997578 - 2017-01-05](https://www.keypedia.com/records/fda_inspections/fivos-inc/155de94d-03a0-421f-a90b-c13b83535684)
- [FDA Inspection 890153 - 2014-08-04](https://www.keypedia.com/records/fda_inspections/fivos-inc/a86d0928-fa37-4de8-aeb0-fb6e049c8de1)

Company: https://www.keypedia.com/companies/fivos-inc/1b74b33c-3afa-4aa2-999b-d02658ccd6e9

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