# FDA Inspection 1079982 - Schiller America, Inc. - February 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 for Schiller America, Inc. on February 19, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1079982 - 2019-02-19](https://www.keypedia.com/records/fda_inspections/schiller-america-inc/1955214e-334a-410d-8a1b-0e29280dcbce)

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