# FDA Inspection 880201 - Vesta Inc. - May 20, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/vesta-inc/97fd79fb-3461-4cf9-a984-9f4e6eaea019
Source feed: FDA_Inspections

> FDA Inspection 880201 for Vesta Inc. on May 20, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 880201
- Company Name: Vesta Inc.
- Inspection Date: 2014-05-20
- 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