FDA inspection
Hologic, Inc.: FDA inspection ending Jan 11, 2007
FDA inspection 455953 · No Action Indicated (NAI) · Bedford, MA
Key facts
| Inspection ID | 455953 |
|---|---|
| Firm | Hologic, Inc. |
| FEI number | 1221300 |
| Address | 35 Crosby Dr |
| City | Bedford |
| State | MA |
| ZIP | 01730-1401 |
| Fiscal year | 2007 |
| Inspection end date | Jan 11, 2007 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med Devices|Compliance: Med 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Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth|Product Evaluation: Med Devices|Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| 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
- 10–99 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