Warning letter
Hydrokinetic Contact Lens Laboratory: warning letter of Nov 7, 2000
FDA warning letter UCM068989 · Dallas District Office
Key facts
| Reference number | UCM068989 |
|---|---|
| Company | Hydrokinetic Contact Lens Laboratory |
| Subject | NewView2 Progressive Addition Contact Lenses/Adulterated/Misbranded |
| Issue date | Nov 7, 2000 |
| Posted date | Nov 7, 2000 |
| Issuing office | Dallas District Office |
| Product type | Devices |
| Country | 3 |
| Inspection city | Houston |
| Inspection ZIP | 77074-5010 |
| Inspection start date | Jul 11, 2000 |
| Letter on fda.gov | web.archive.org |
At a glance
- 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: