# KATALYST, Inc. – FDA Inspection, Mar 28, 2019

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

> FDA inspection 1084222 of KATALYST, Inc., March 28, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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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)
- 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: 1

## Related Officers

- [Company Rep](https://www.keypedia.com/people/christopher-s-genther/e71df42c-9adf-4a78-93e5-c364dcc06b35)

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

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