# FDA Inspection 983522 - Holger Bumueller LLC - September 13, 2016

Source: https://www.keypedia.com/records/fda_inspections/holger-bumueller-llc/6ac2184b-28b9-49a1-afdc-054eb75de6a0
Source feed: FDA_Inspections

> FDA Inspection 983522 for Holger Bumueller LLC on September 13, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 983522
- Company Name: Holger Bumueller LLC
- Inspection Date: 2016-09-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 983522 - 2016-09-13](https://www.keypedia.com/records/fda_inspections/holger-bumueller-llc/1492b578-b368-4cc8-838c-4b44b26694af)

Company: https://www.keypedia.com/companies/holger-bumueller-llc/23e2755e-2d33-4c6e-aaf1-a61f2cf3aaf1

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