Warning letter
Oculo-Plastik, Inc.: warning letter of Dec 22, 2015
FDA warning letter UCM512405 · Center for Devices and Radiological Health
Key facts
| Reference number | UCM512405 |
|---|---|
| Company | Oculo-Plastik, Inc. |
| Subject | CGMP/Finished Pharmaceuticals/Adulterated |
| Issue date | Dec 22, 2015 |
| Posted date | Dec 22, 2015 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 820, 820.40 |
| 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: