# Schiller Medical – FDA Inspection, Mar 22, 2018

Source: https://www.keypedia.com/records/fda_inspections/schiller-medical/444a5a3c-a521-4245-a0c5-c873f8b4943a
Source feed: FDA_Inspections

> FDA inspection 1045200 of Schiller Medical, March 22, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1045200
- Company Name: Schiller Medical
- Inspection Date: 2018-03-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [Company Rep](https://www.keypedia.com/people/paul-m-kawamoto/0a24b110-12de-4736-8d98-7a023ceec01e)

Company: https://www.keypedia.com/companies/schiller-medical/85056ed3-bb7d-4132-af2e-9581ab6b5119

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