# FDA Inspection 897353 - The EF Precision Group - September 25, 2014

Source: https://www.keypedia.com/records/fda_inspections/the-ef-precision-group/c04fa3cf-ac29-4443-bba0-c0a2dba13c40
Source feed: FDA_Inspections

> FDA Inspection 897353 for The EF Precision Group on September 25, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 897353
- Company Name: The EF Precision Group
- Inspection Date: 2014-09-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1145274 - 2021-07-02](https://www.keypedia.com/records/fda_inspections/the-ef-precision-group/b9ba4d8a-345e-4b5b-95f3-adeac1d7b075)
- [FDA Inspection 897353 - 2014-09-25](https://www.keypedia.com/records/fda_inspections/the-ef-precision-group/31a7a083-501f-4083-904a-59e63fba6f3c)

Company: https://www.keypedia.com/companies/the-ef-precision-group/57ec06ac-8093-423d-a536-51d6899ff9ca

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