FDA inspection
Abbott Vascular Costa Rica (AVCR): FDA inspection ending May 9, 2013
FDA inspection 832772 · Administrative/Directed Change (ADC) · El Coyol, Alajuela
Key facts
| Inspection ID | 832772 |
|---|---|
| Firm | Abbott Vascular Costa Rica (AVCR) |
| FEI number | 3009564766 |
| Address | 52 Calle 3, B31 Coyol Free Zone, Calle 3, Coyol Free Zone 52 |
| City | El Coyol, Alajuela |
| Fiscal year | 2013 |
| Inspection end date | May 9, 2013 |
| Classification | Administrative/Directed Change (ADC) |
| 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: 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 Devices|Compliance: Medical 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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 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 |
| 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