Warning letter
Abbott (St Jude Medical Inc.): warning letter of Apr 12, 2017
FDA warning letter 519686 · Center for Devices and Radiological Health
Key facts
| Reference number | 519686 |
|---|---|
| Company | Abbott (St Jude Medical Inc.) |
| Subject | CGMP/QSR/Manufacture/Packing/Storage/Installation/Adulterated |
| Issue date | Apr 12, 2017 |
| Posted date | Apr 12, 2017 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 820 |
| Inspection city | Sylmar |
| Inspection ZIP | 91342 |
| Inspection start date | Feb 7, 2017 |
| Letter on fda.gov | fda.gov |
At a glance
- 1–9 CFR sections cited
- OAI Linked inspection classification
- Yes Form FDA 483 issued
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA warning letters
FDA warning letters notify a firm of significant regulatory violations found during an inspection or review and request prompt corrective action.
Source: U.S. Food and Drug Administration (FDA), Warning Letters · Source date: