# FDA Inspection 880230 - Hausmann Industries, Inc. - May 27, 2014

Source: https://www.keypedia.com/records/fda_inspections/hausmann-industries-inc/bc59780b-6fdf-4b07-bf3e-7d5fe4b609b2
Source feed: FDA_Inspections

> FDA Inspection 880230 for Hausmann Industries, Inc. on May 27, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 880230
- Company Name: Hausmann Industries, Inc.
- Inspection Date: 2014-05-27
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 880230 - 2014-05-27](https://www.keypedia.com/records/fda_inspections/hausmann-industries-inc/e635a011-3fd9-4d2d-8c67-6d6b3c193c12)

Company: https://www.keypedia.com/companies/hausmann-industries-inc/4a20529f-c7e3-4b7d-b7ce-bfa5b0d0ebda

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7