FDA inspection
Hologic Inc: FDA inspection ending Feb 15, 2024
FDA inspection 1230813 · No Action Indicated (NAI) · Newark, DE
Key facts
| Inspection ID | 1230813 |
|---|---|
| Firm | Hologic Inc |
| FEI number | 3005496266 |
| Address | 600 Technology Dr |
| City | Newark |
| State | DE |
| ZIP | 19702-2463 |
| Fiscal year | 2024 |
| Inspection end date | Feb 15, 2024 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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