Warning letter
Cantor & Nissel Ltd. [ARCHIVED]: warning letter of Sep 27, 2011
FDA warning letter 207433 · Center for Devices and Radiological Health
Key facts
| Reference number | 207433 |
|---|---|
| Company | Cantor & Nissel Ltd. [ARCHIVED] |
| Subject | Adulterated Device/Misbranding/Quality Control |
| Issue date | Sep 27, 2011 |
| Posted date | Sep 27, 2011 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 803, 803.3, 803.17, 803.19, 803.50, 803.17(a)(1), 820, 803.18(d), 803.50(a), 803.50(b)(3) |
| Inspection city | Brackley |
| Inspection start date | Apr 26, 2011 |
| Letter on fda.gov | web.archive.org |
At a glance
- 10–99 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: