FDA inspection
Novadaq Technologies, Inc.: FDA inspection ending Jun 12, 2014
FDA inspection 886175 · No Action Indicated (NAI) · Richmond
Key facts
| Inspection ID | 886175 |
|---|---|
| Firm | Novadaq Technologies, Inc. |
| FEI number | 3008177327 |
| Address | 13155 Delf Place |
| City | Richmond |
| Fiscal year | 2014 |
| Inspection end date | Jun 12, 2014 |
| 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 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: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: 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Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical 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Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Compliance: Medical Devices|Product Evaluation: Med Devices|Product Evaluation: Medical 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| 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