FDA inspection
ZOLL Medical Corporation: FDA inspection ending Jul 24, 2025
FDA inspection 1276399 · Voluntary Action Indicated (VAI) · Wilmington, Massachusetts
Key facts
| Inspection ID | 1276399 |
|---|---|
| Firm | ZOLL Medical Corporation |
| FEI number | 3038259592 |
| Address | 38 Upton Dr |
| City | Wilmington |
| State | Massachusetts |
| ZIP | 01887 |
| Fiscal year | 2025 |
| Inspection end date | Jul 24, 2025 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Medical 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