# Gobiquity, Inc – FDA Inspection, Aug 17, 2018

Source: https://www.keypedia.com/records/fda_inspections/gobiquity-inc/b3465be5-9c72-41de-9d3e-f36bce184b0e
Source feed: FDA_Inspections

> FDA inspection 1062903 of Gobiquity, Inc, August 17, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1062903
- Company Name: Gobiquity, Inc
- Inspection Date: 2018-08-17
- 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

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/maksim-a-levenchuk/d77c93d7-d86e-4df8-b803-abae068a4dd2)

Company: https://www.keypedia.com/companies/gobiquity-inc/d3a6698c-d438-4e5b-a7cb-d10e8882eceb

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