Warning letter
Sonar Products, Inc.: warning letter of Aug 28, 2001
FDA warning letter UCM178618 · New Jersey District Office
Key facts
| Reference number | UCM178618 |
|---|---|
| Company | Sonar Products, Inc. |
| Subject | GMP for Finished Pharmaceuticals/Prescription & Over-the-Counter Products |
| Issue date | Aug 28, 2001 |
| Posted date | Aug 28, 2001 |
| Issuing office | New Jersey District Office |
| Product type | Devices |
| Country | 3 |
| Inspection city | Carlstadt |
| Inspection ZIP | 07072-1611 |
| Inspection start date | Jul 18, 2001 |
| Letter on fda.gov | web.archive.org |
At a glance
- 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: