FDA Inspection 1220305 — Pulse Technologies, Inc
The FDA completed an inspection of Pulse Technologies, Inc on September 21, 2023 in Quakertown, PA. 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
- September 21, 2023
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Quakertown, PA (United States)