# FDA Inspection 1030227 - Vesta Inc. - October 20, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/vesta-inc/3f96f6fa-5030-4cf4-855b-79d086d4dc8d
Source feed: FDA_Inspections

> FDA Inspection 1030227 for Vesta Inc. on October 20, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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