# FDA Inspection 1220305 - Pulse Technologies, Inc - September 21, 2023

Source: https://www.keypedia.com/records/fda_inspections/pulse-technologies-inc/66ba2997-8f2f-427b-9339-0ebc0ad58d25
Source feed: FDA_Inspections

> FDA Inspection 1220305 for Pulse Technologies, Inc on September 21, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1220305
- Company Name: Pulse Technologies, Inc
- Inspection Date: 2023-09-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/pulse-technologies-inc/9aaf0555-87c2-46a6-8033-00dc4270e643

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