# FDA 483 - The EF Precision Group - July 02, 2021

Source: https://www.keypedia.com/records/483/the-ef-precision-group/fd3622f2-d9f1-43e7-a0a0-b38740e532cb

> FDA 483 for The EF Precision Group on July 02, 2021. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: The EF Precision Group
- Inspection Date: 2021-07-02
- Product Type: device
- Office Name: Philadelphia District Office
- Summary: An FDA inspection of The EF Precision Group, a contract manufacturer in Willow Grove, PA, revealed two significant issues. The firm failed to adequately document corrective and preventive action activities, specifically regarding the verification of effectiveness for several corrective actions. Additionally, the company did not document and approve process validation activities, particularly for a cleaning process used on manufactured parts.

## Related Officers

- [Consumer Safety Officer](https://www.keypedia.com/people/suzanne-m-healy/a4159f42-8968-4dec-89e3-46a5412bc47a)

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

Office: https://www.keypedia.com/offices/philadelphia-district-office/c5ec7398-b3d5-4125-9793-fb7b972578d8