FDA Inspection
Apollo CorpApollo Corp – FDA Inspection, Sep 7, 2017
Record Details
This FDA Inspection record concerns Apollo Corp, with an inspection on September 7, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 454f3d71-bb65-43b4-8b8a-b9f7a7ea6741
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1024802
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.198(a)Complaints
- 21 CFR 820.198(b)Rationale documented for no investigation
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Other FDA inspections of Apollo Corp
3| Date | Classification | Office | Project area |
|---|---|---|---|
| May 9, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 24, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 14, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Apollo Corp
- FDA Inspection 1171413 - 2022-05-09
- FDA Inspection 804647 - 2012-10-24
- FDA Inspection 659217 - 2010-04-14
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