# Apollo Corp – FDA Inspection, Sep 7, 2017

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

> FDA inspection 1024802 of Apollo Corp, September 07, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1171413 - 2022-05-09
- FDA Inspection 804647 - 2012-10-24
- FDA Inspection 659217 - 2010-04-14

## Related Officers

- [Company Rep](https://www.keypedia.com/people/joseph-d-gong/c1079a56-5f84-4e0d-9f76-9dc1187e588a)

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