Warning letter
Progeny, Inc.: warning letter of Jul 19, 2001
FDA warning letter UCM178302 · Chicago District Office
Key facts
| Reference number | UCM178302 |
|---|---|
| Company | Progeny, Inc. |
| Subject | Medical Device Corrections and Removals/Misbranded |
| Issue date | Jul 19, 2001 |
| Posted date | Jul 19, 2001 |
| Issuing office | Chicago District Office |
| Product type | Devices |
| CFR sections cited | 806.10(a), 806, 820 |
| Country | 3 |
| Inspection city | Buffalo Grove |
| Inspection ZIP | 60089-4528 |
| Inspection start date | Mar 6, 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: