# FDA Inspection 1024802 - Apollo Corp - September 07, 2017

Source: https://www.keypedia.com/records/fda_inspections/apollo-corp/454f3d71-bb65-43b4-8b8a-b9f7a7ea6741
Source feed: FDA_Inspections

> FDA Inspection 1024802 for Apollo Corp on September 07, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024802
- Company Name: Apollo Corp
- 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/apollo-corp/15265f06-b588-44ed-8423-fae2a637d1cb

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