# FDA Inspection 980176 - Scholly Fiberoptic Gmbh - June 30, 2016

Source: https://www.keypedia.com/records/fda_inspections/scholly-fiberoptic-gmbh/c3e1b36c-cbe6-484f-af5c-998896e2e2c8
Source feed: FDA_Inspections

> FDA Inspection 980176 for Scholly Fiberoptic Gmbh on June 30, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980176
- Company Name: Scholly Fiberoptic Gmbh
- Inspection Date: 2016-06-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 838580 - 2013-06-06](https://www.keypedia.com/records/fda_inspections/scholly-fiberoptic-gmbh/930c08f2-95cd-4c0a-ade0-1009273d4920)
- [FDA Inspection 838580 - 2013-06-06](https://www.keypedia.com/records/fda_inspections/scholly-fiberoptic-gmbh/20e5b161-274e-4046-a8c9-edaa47e0cbfd)

Company: https://www.keypedia.com/companies/scholly-fiberoptic-gmbh/cb758253-2f29-488f-95d0-5e0dda3a157e

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