FDA inspection
Guardant Health, Inc: FDA inspection ending Jun 29, 2023
FDA inspection 1210058 · No Action Indicated (NAI) · Redwood City, California
Key facts
| Inspection ID | 1210058 |
|---|---|
| Firm | Guardant Health, Inc |
| FEI number | 3012090384 |
| Address | 505 Penobscot Dr |
| City | Redwood City |
| State | California |
| ZIP | 94063 |
| Fiscal year | 2023 |
| Inspection end date | Jun 29, 2023 |
| Classification | No Action Indicated (NAI) |
| 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: 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: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: 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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: 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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|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
- 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