Warning letter
Bracco Diagnostics Inc: warning letter of Jan 31, 2012
FDA warning letter 210573 · New Jersey District Office
Key facts
| Reference number | 210573 |
|---|---|
| Company | Bracco Diagnostics Inc |
| Subject | CGMP/Finished Pharmaceuticals/Adulterated |
| Issue date | Jan 31, 2012 |
| Posted date | Jan 31, 2012 |
| Issuing office | New Jersey District Office |
| Product type | Drugs |
| CFR sections cited | 211.192 |
| Inspection city | Princeton |
| Inspection ZIP | 08540 |
| Inspection start date | Jun 23, 2011 |
| 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: