Warning letter
Farouk Systems, Inc.: warning letter of Aug 1, 2001
FDA warning letter UCM178378 · Dallas District Office
Key facts
| Reference number | UCM178378 |
|---|---|
| Company | Farouk Systems, Inc. |
| Subject | Current Good Manufacturing Practices for Finished Pharmaceuticals/Adulterated |
| Issue date | Aug 1, 2001 |
| Posted date | Aug 1, 2001 |
| Issuing office | Dallas District Office |
| Product type | Drugs |
| CFR sections cited | 211.198, 211.25(a), 21, 211.22, 211.122 |
| Country | 3 |
| Inspection city | Houston |
| Inspection ZIP | 77090-5905 |
| Inspection start date | May 29, 2001 |
| 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: