# FDA Inspection 1211449 - Ackermann Usa Inc - August 04, 2023

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

> FDA Inspection 1211449 for Ackermann Usa Inc on August 04, 2023. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1211449 - 2023-08-04](https://www.keypedia.com/records/fda_inspections/ackermann-usa-inc/54509641-ddfc-4840-89bc-b6fd422afe69)

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