FDA Inspection 1336660 — Impulse Dynamics (USA), Inc.

Impulse Dynamics (USA), Inc. — FEI 3017555074

The FDA completed an inspection of Impulse Dynamics (USA), Inc. on Sep 3, 2026 in Marlton, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 3, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Marlton, NJ (United States)

Additional Details

Sponsor, Contract Research Organization

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.