# Ackermann Usa Inc – FDA Inspection, Aug 4, 2023

Source: https://www.keypedia.com/records/fda_inspections/ackermann-usa-inc/e45576bb-436c-4fe7-9f5f-488fe2d0302b
Source feed: FDA_Inspections

> FDA inspection 1211449 of Ackermann Usa Inc, August 04, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1211449
- Company Name: Ackermann Usa Inc
- Inspection Date: 2023-08-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [Issuing Officer](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/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7