FDA Inspection 1010935 — Impulse Dynamics (USA), Inc.
The FDA completed an inspection of Impulse Dynamics (USA), Inc. on May 18, 2017 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
- May 18, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Pearl River, NY (United States)