# The Prometheus Group – FDA Inspection, Jun 21, 2012

Source: https://www.keypedia.com/records/fda_inspections/the-prometheus-group/b3e4d91b-5bde-413b-a3dd-63ffd65123f1
Source feed: FDA_Inspections

> FDA inspection 787543 of The Prometheus Group, June 21, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 787543
- Company Name: The Prometheus Group
- Inspection Date: 2012-06-21
- 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 1002606 - 2017-02-15
- [FDA Inspection 891411 - 2014-08-18](https://www.keypedia.com/records/fda_inspections/the-prometheus-group/108c2e78-bd4e-4ae0-9e83-9f9730f9e3e3)
- [FDA Inspection 667399 - 2010-06-02](https://www.keypedia.com/records/fda_inspections/the-prometheus-group/30f73338-9f83-49c0-b128-91b8652592a7)

Company: https://www.keypedia.com/companies/the-prometheus-group/511e29e0-ce1c-43bb-9240-754d96429c0a

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