FDA Inspection 772328 — Impulse Dynamics (USA), Inc.

Impulse Dynamics (USA), Inc. — FEI 3007805252

The FDA completed an inspection of Impulse Dynamics (USA), Inc. on February 24, 2012 in Pearl River, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 24, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Pearl River, NY (United States)