# FDA 483 - Allen Milling Technologies - November 17, 2020

Source: https://www.keypedia.com/records/483/allen-milling-technologies/4b862df7-c856-442d-aa52-c8fb19071757

> FDA 483 for Allen Milling Technologies on November 17, 2020. Product: device. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: Allen Milling Technologies
- Inspection Date: 2020-11-17
- Product Type: device
- Office Name: Division of Pharmaceutical Quality Operations IV
- Summary: An FDA inspection of Allen Milling Technologies, a medical device manufacturer in Glendora, CA, revealed significant deficiencies in their quality system. Observations included a lack of documented personnel training, failure to conduct internal quality audits, and inadequate documentation of acceptance activities for both incoming and finished products. These issues indicate a fundamental breakdown in adherence to established procedures and quality control.

## Related Officers

- [Linda Galindo](https://www.keypedia.com/people/linda-galindo/6bc29df6-192b-4d89-92ae-20cc1660d9ad)

Company: https://www.keypedia.com/companies/allen-milling-technologies/38e7971f-560c-4819-ba07-41f7cb9cab51

Office: https://www.keypedia.com/offices/division-of-pharmaceutical-quality-operations-iv/a2d2ff91-dc0f-433e-b91f-ca90ff8998b6