# FDA 483 - Hanza - September 21, 2021

Source: https://www.keypedia.com/records/483/hanza/5c36f3e5-cb36-413b-a4d4-1d68f6c0658b

> FDA 483 for Hanza on September 21, 2021. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Hanza
- Inspection Date: 2021-09-21
- Product Type: other
- Office Name: Minneapolis District Office
- Summary: Hanza, a nonclinical laboratory in Minneapolis, MN, was inspected by the FDA, resulting in one observation. The firm failed to retain all required documentation records, raw data, and specimens from nonclinical laboratory studies in the archives for the appropriate time. This practice was contrary to GLP retention requirements and firm procedures.

## Related Officers

- [investigator](https://www.keypedia.com/people/nicole-c-victoria/8c5f8060-452f-4fe5-a43f-a448ec020e60)

Company: https://www.keypedia.com/companies/hanza/de577b50-2eb4-48af-8f54-6d72ce3a22b0

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d