Warning letter
Tri-State Analytical Laboratory LLC: warning letter of Oct 22, 2003
FDA warning letter UCM147789 · New Orleans District Office
Key facts
| Reference number | UCM147789 |
|---|---|
| Company | Tri-State Analytical Laboratory LLC |
| Subject | GMP for Finished Pharmaceuticals/Adulterated |
| Issue date | Oct 22, 2003 |
| Posted date | Oct 22, 2003 |
| Issuing office | New Orleans District Office |
| Product type | Drugs |
| CFR sections cited | 211.165(a), 211.165(e), 211.160(b), 211.194(c) |
| Country | 3 |
| Inspection city | Johnson City |
| Inspection ZIP | 37604-6274 |
| Inspection start date | Jul 23, 2003 |
| 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: