# FDA Inspection 1028757 - Wright - September 07, 2017

Source: https://www.keypedia.com/records/fda_inspections/wright/08638c68-352e-4a13-a4d1-9a36bbd58c4a
Source feed: FDA_Inspections

> FDA Inspection 1028757 for Wright on September 07, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028757
- Company Name: Wright
- Inspection Date: 2017-09-07
- 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.keypedia.com/companies/wright/044b3f2c-b161-47ca-80eb-822b9ffe83d2

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