# FDA Inspection 931850 - Hanson & Zollinger Inc. - June 26, 2015

Source: https://www.keypedia.com/records/fda_inspections/hanson-zollinger-inc/454181cd-b922-4879-8f4a-42eb07dc9689
Source feed: FDA_Inspections

> FDA Inspection 931850 for Hanson & Zollinger Inc. on June 26, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 931850
- Company Name: Hanson & Zollinger Inc.
- Inspection Date: 2015-06-26
- 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 931850 - 2015-06-26](https://www.keypedia.com/records/fda_inspections/hanson-zollinger-inc/b4669c86-fe5f-49e4-8b6f-ba9642355183)

Company: https://www.keypedia.com/companies/hanson-zollinger-inc/e3bb1c08-766c-40aa-aff4-676743132af4

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