Warning letter
Zeus Scientific Inc.: warning letter of Mar 27, 2001
FDA warning letter UCM069480 · New Jersey District Office
Key facts
| Reference number | UCM069480 |
|---|---|
| Company | Zeus Scientific Inc. |
| Subject | IVD Test Kits/Reporting Requirements |
| Issue date | Mar 27, 2001 |
| Posted date | Mar 27, 2001 |
| Issuing office | New Jersey District Office |
| Product type | Devices |
| CFR sections cited | 806 |
| Country | 3 |
| Inspection city | Branchburg |
| Inspection ZIP | 08876-4600 |
| Inspection start date | Jan 16, 2001 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- VAI 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: