# FDA Inspection 930130 - SUBAN Instruments Germany GmbH - May 05, 2015

Source: https://www.keypedia.com/records/fda_inspections/suban-instruments-germany-gmbh/9b777a5c-8345-48c1-a78c-7403d271cd3b
Source feed: FDA_Inspections

> FDA Inspection 930130 for SUBAN Instruments Germany GmbH on May 05, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 930130
- Company Name: SUBAN Instruments Germany GmbH
- Inspection Date: 2015-05-05
- 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 930130 - 2015-05-05](https://www.keypedia.com/records/fda_inspections/suban-instruments-germany-gmbh/3f665623-224d-4b1c-80e0-237b410cd068)

Company: https://www.keypedia.com/companies/suban-instruments-germany-gmbh/27a89cd9-ee4e-41ff-918b-e0c6d4e2ddf4

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