Warning letter
Patterson Technology Center, Inc.: warning letter of Oct 24, 2006
FDA warning letter UCM076137 · Chicago District Office
Key facts
| Reference number | UCM076137 |
|---|---|
| Company | Patterson Technology Center, Inc. |
| Subject | CGMP Requirements of Medical Device Reporting/Misbranded/Adulterated |
| Issue date | Oct 24, 2006 |
| Posted date | Oct 24, 2006 |
| Issuing office | Chicago District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.17, 820, 820.40 |
| Country | 3 |
| Inspection city | Effingham |
| Inspection ZIP | 62401-4660 |
| Inspection start date | May 15, 2006 |
| 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: