Warning letter
Abbott Laboratories: warning letter of Aug 7, 2000
FDA warning letter UCM068704 · Chicago District Office
Key facts
| Reference number | UCM068704 |
|---|---|
| Company | Abbott Laboratories |
| Subject | Medical Device Corrections and Removals/Infusion Pumps |
| Issue date | Aug 7, 2000 |
| Posted date | Aug 7, 2000 |
| Issuing office | Chicago District Office |
| Product type | Devices |
| CFR sections cited | 806, 806.10(a)(1), 806.10(a) |
| Country | 3 |
| Inspection city | Abbott Park |
| Inspection ZIP | 60064-3502 |
| Inspection start date | Mar 20, 2000 |
| Letter on fda.gov | web.archive.org |
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: