# Fivos, Inc. – FDA Inspection, Aug 4, 2014

Source: https://www.keypedia.com/records/fda_inspections/fivos-inc/a86d0928-fa37-4de8-aeb0-fb6e049c8de1
Source feed: FDA_Inspections

> FDA inspection 890153 of Fivos, Inc., August 04, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 890153
- Company Name: Fivos, Inc.
- Inspection Date: 2014-08-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1110192 - 2019-11-07
- FDA Inspection 997578 - 2017-01-05

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