# FDA Inspection 1018320 - Dr. Gernot Schuhfried Ges.m.b.H. - May 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/dr-gernot-schuhfried-gesmbh/bb5f7fcb-1fe6-483f-998a-6f8533d4c958
Source feed: FDA_Inspections

> FDA Inspection 1018320 for Dr. Gernot Schuhfried Ges.m.b.H. on May 18, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018320
- Company Name: Dr. Gernot Schuhfried Ges.m.b.H.
- Inspection Date: 2017-05-18
- 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 1018320 - 2017-05-18](https://www.keypedia.com/records/fda_inspections/dr-gernot-schuhfried-gesmbh/539e2302-f8f6-4315-bc87-861b95235fd8)

Company: https://www.keypedia.com/companies/dr-gernot-schuhfried-gesmbh/c24dfba1-1923-4426-9697-2ce2956461d1

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