# Dr. Gernot Schuhfried Ges.m.b.H. – FDA Inspection, 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 of Dr. Gernot Schuhfried Ges.m.b.H., May 18, 2017. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Officers

- [Investigator](https://www.keypedia.com/people/kathleen-s-tormey/5e1abfe2-078a-4c61-bb98-3885f853a945)

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