# Vesta Inc. – FDA Inspection, Oct 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/vesta-inc/ddc20b10-f0f1-4d97-859d-18a911075def
Source feed: FDA_Inspections

> FDA inspection 1030227 of Vesta Inc., October 20, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030227
- Company Name: Vesta Inc.
- Inspection Date: 2017-10-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: 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/michelle-j-glembin/e58f4652-d09f-41a7-941d-335c7b5338ad)

Company: https://www.keypedia.com/companies/vesta-inc/3ae5130d-4835-46fb-b93c-4f1c1e59c18e

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