Warning letter
Medco Instruments Inc.: warning letter of Jun 9, 2000
FDA warning letter UCM068502 · Chicago District Office
Key facts
| Reference number | UCM068502 |
|---|---|
| Company | Medco Instruments Inc. |
| Subject | Medical Device Reporting/Circumcision Clamps |
| Issue date | Jun 9, 2000 |
| Posted date | Jun 9, 2000 |
| Issuing office | Chicago District Office |
| Product type | Devices |
| CFR sections cited | 803.17, 803.50(a), 803, 820, 806, 803.50(a)(1), 803.50(b)(2), 803.18 |
| Country | 3 |
| Inspection city | Hickory Hills |
| Inspection ZIP | 60457-2234 |
| Inspection start date | Jan 11, 2000 |
| 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: