# FDA Inspection 981515 - Helmut Zepf Medizintechnik Gmbh - July 13, 2016

Source: https://www.keypedia.com/records/fda_inspections/helmut-zepf-medizintechnik-gmbh/824d581c-e32f-45e0-83ec-111840e0629d
Source feed: FDA_Inspections

> FDA Inspection 981515 for Helmut Zepf Medizintechnik Gmbh on July 13, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 981515
- Company Name: Helmut Zepf Medizintechnik Gmbh
- Inspection Date: 2016-07-13
- 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 981515 - 2016-07-13](https://www.keypedia.com/records/fda_inspections/helmut-zepf-medizintechnik-gmbh/262c4c8c-90f5-4441-8fc5-a47f7726ecd1)

Company: https://www.keypedia.com/companies/helmut-zepf-medizintechnik-gmbh/46419cd6-d198-4efc-ab4b-21a6a5902cf0

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