# FDA Inspection 1002606 - The Prometheus Group - February 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/the-prometheus-group/0e6307e9-4f11-41a4-9f3b-6d538e1a63bf
Source feed: FDA_Inspections

> FDA Inspection 1002606 for The Prometheus Group on February 15, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002606
- Company Name: The Prometheus Group
- Inspection Date: 2017-02-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 891411 - 2014-08-18](https://www.keypedia.com/records/fda_inspections/the-prometheus-group/108c2e78-bd4e-4ae0-9e83-9f9730f9e3e3)
- [FDA Inspection 787543 - 2012-06-21](https://www.keypedia.com/records/fda_inspections/the-prometheus-group/b3e4d91b-5bde-413b-a3dd-63ffd65123f1)
- [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