Warning letter
Microline Inc.: warning letter of May 20, 1999
FDA warning letter UCM067365 · New England District Office
Key facts
| Reference number | UCM067365 |
|---|---|
| Company | Microline Inc. |
| Subject | Quality System Regulation/Re-New II Hybrid Laparascopic Instruments |
| Issue date | May 20, 1999 |
| Posted date | May 20, 1999 |
| Issuing office | New England District Office |
| Product type | Devices |
| CFR sections cited | 803.50(a)(1), 820 |
| Country | 3 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
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: