# FDA Inspection 1084222 - KATALYST, Inc. - March 28, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/katalyst-inc/f8a8de21-441a-47b8-972a-4c25b9bb23a3/
Source feed: FDA_Inspections

> FDA Inspection 1084222 for KATALYST, Inc. on March 28, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1084222
- Company Name: KATALYST, Inc.
- Inspection Date: 2019-03-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1084222 - 2019-03-28](https://www.globalkeysolutions.net/api/records/fda_inspections/katalyst-inc/aab9fe7a-8016-4b4e-b98a-9b552928168c/)

Company: https://www.globalkeysolutions.net/companies/katalyst-inc/c63e76d8-47c8-41a5-b2b5-8e0e373cc730

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