# FDA 483 - Ackermann Usa Inc - August 04, 2023

Source: https://www.keypedia.com/records/483/ackermann-usa-inc/e145ce26-13bb-4b3d-8cbe-a84f5f26187f

> FDA 483 for Ackermann Usa Inc on August 04, 2023. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Ackermann Usa Inc
- Inspection Date: 2023-08-04
- Product Type: device
- Office Name: Division of Human and Animal Food Operations - East I
- Summary: Ackermann Usa Inc, a manufacturer in Bayport, NY, was issued a Form FDA 483 with two observations following an inspection. The inspection revealed a lack of established written procedures for handling customer complaints and for the acceptance of incoming finished devices. These deficiencies indicate issues within the firm's quality system.

## Related Officers

- [Andrew J. Garufi](https://www.keypedia.com/people/andrew-j-garufi/567f6aaa-f6f2-45a3-9a58-80b33f3ad021)

Company: https://www.keypedia.com/companies/ackermann-usa-inc/2348cba9-f268-469c-9971-662dc5da7ab7

Office: https://www.keypedia.com/offices/division-of-human-and-animal-food-operations-east-i/a807f00e-d780-40b8-b233-1eb92ece8961