# Schiller America, Inc. – FDA Inspection, Feb 19, 2019

Source: https://www.keypedia.com/records/fda_inspections/schiller-america-inc/ed1ec2b9-7f01-4412-b59b-02adf03b31ef
Source feed: FDA_Inspections

> FDA inspection 1079982 of Schiller America, Inc., February 19, 2019. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079982
- Company Name: Schiller America, Inc.
- Inspection Date: 2019-02-19
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stanley-b-eugene/4708f43e-0592-4c24-b276-d9f9092788a3)

Company: https://www.keypedia.com/companies/schiller-america-inc/0c713ac5-0d30-4936-886b-ff38badd97bd

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