# FDA Inspection 1102359 - ERI Group - September 20, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/eri-group/dd840304-fb92-4742-9025-d49e2db60b81
Source feed: FDA_Inspections

> FDA Inspection 1102359 for ERI Group on September 20, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102359
- Company Name: ERI Group
- Inspection Date: 2019-09-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1102359 - 2019-09-20](https://www.globalkeysolutions.net/records/fda_inspections/eri-group/3be3b113-bcf5-42be-bc61-582753d68665)

Company: https://www.globalkeysolutions.net/companies/eri-group/3d52d397-5b04-40a3-9fb3-b5c404175af1

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