# FDA Inspection 1314736 - Praxis Powder Technology, Inc. - April 30, 2026

Source: https://www.keypedia.com/records/fda_inspections/praxis-powder-technology-inc/2a267fb3-4e42-4be0-870c-0f25440e924d
Source feed: FDA_Inspections

> FDA Inspection 1314736 for Praxis Powder Technology, Inc. on April 30, 2026. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1314736
- Company Name: Praxis Powder Technology, Inc.
- Inspection Date: 2026-04-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New York District Office

## Related Documents

- [FDA Inspection 1175988 - 2022-07-29](https://www.keypedia.com/records/fda_inspections/praxis-powder-technology-inc/3069fed7-873b-4794-aa65-591e8d4ae0ce)
- [FDA Inspection 1111048 - 2019-10-31](https://www.keypedia.com/records/fda_inspections/praxis-powder-technology-inc/5125d23f-57c6-4e7e-b458-879c801a8cf1)

Company: https://www.keypedia.com/companies/praxis-powder-technology-inc/2524d7e2-13c3-49dc-bd11-f5964a8e57eb

Office: https://www.keypedia.com/offices/new-york-district-office/9fa3d265-16ca-438d-8a6e-b47f60dc260d