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

Source: https://www.keypedia.com/records/fda_inspections/katalyst-inc/aab9fe7a-8016-4b4e-b98a-9b552928168c
Source feed: FDA_Inspections

> FDA Inspection 1084222 for KATALYST, Inc. on March 28, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1084222
- Company Name: KATALYST, Inc.
- Inspection Date: 2019-03-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1084222 - 2019-03-28](https://www.keypedia.com/records/fda_inspections/katalyst-inc/f8a8de21-441a-47b8-972a-4c25b9bb23a3)

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