# FDA Inspection 994023 - West-Ward Columbus Inc - October 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/west-ward-columbus-inc/049e65cd-6660-46f4-964c-d43e607f0461
Source feed: FDA_Inspections

> FDA Inspection 994023 for West-Ward Columbus Inc on October 21, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 994023
- Company Name: West-Ward Columbus Inc
- Inspection Date: 2016-10-21
- 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/west-ward-columbus-inc/6289cb89-1444-49a0-91b0-75a04e5152eb

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