Warning letter
KBD, Inc. [ARCHIVED]: warning letter of Dec 15, 2011
FDA warning letter 216414 · Cincinnati District Office
Key facts
| Reference number | 216414 |
|---|---|
| Company | KBD, Inc. [ARCHIVED] |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Dec 15, 2011 |
| Posted date | Dec 15, 2011 |
| Issuing office | Cincinnati District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.17, 820, 1040.20 |
| Inspection city | North Las Vegas |
| Inspection ZIP | 89032 |
| Inspection start date | Jul 5, 2011 |
| 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: