Warning letter
Biomet, Inc.: warning letter of Jul 27, 2010
FDA warning letter 93168 · Center for Devices and Radiological Health
Key facts
| Reference number | 93168 |
|---|---|
| Company | Biomet, Inc. |
| Subject | Premarket Approval/Misbranded/Adulterated |
| Issue date | Jul 27, 2010 |
| Posted date | Jul 27, 2010 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 807.81(b) |
| Country | 1 |
| 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: