FDA inspection
PureWave Life LLC: FDA inspection ending Apr 29, 2026
FDA inspection 1314952 · Voluntary Action Indicated (VAI) · Boynton Beach, FL
Key facts
| Inspection ID | 1314952 |
|---|---|
| Firm | PureWave Life LLC |
| FEI number | 3015195058 |
| Address | 3497 High Ridge Rd |
| City | Boynton Beach |
| State | FL |
| ZIP | 33426 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Apr 29, 2026 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data