# FDA Inspection 1020077 - Ziehm Imaging Inc. - August 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/ziehm-imaging-inc/f3818e63-8016-4651-968b-57701fffe272
Source feed: FDA_Inspections

> FDA Inspection 1020077 for Ziehm Imaging Inc. on August 02, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020077
- Company Name: Ziehm Imaging Inc.
- Inspection Date: 2017-08-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1020077 - 2017-08-02](https://www.keypedia.com/records/fda_inspections/ziehm-imaging-inc/fc558f1a-bf07-41d4-8c25-5d3c268b269a)
- [FDA Inspection 1020077 - 2017-08-02](https://www.keypedia.com/records/fda_inspections/ziehm-imaging-inc/718b43ef-4f7f-452c-92f5-9d4352612d21)

Company: https://www.keypedia.com/companies/ziehm-imaging-inc/9b7c95aa-d547-410c-ae65-c4d0ddd8d0a4

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