Warning letter
Okamoto Rubber Products Co., Ltd. [ARCHIVED]: warning letter of Dec 30, 2011
FDA warning letter 254174 · Center for Devices and Radiological Health
Key facts
| Reference number | 254174 |
|---|---|
| Company | Okamoto Rubber Products Co., Ltd. [ARCHIVED] |
| Subject | Medical Device Reporting/Misbranded |
| Issue date | Dec 30, 2011 |
| Posted date | Dec 30, 2011 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 803.17, 803.20(c)(1), 820, 803.50, 803, 803.3 |
| Inspection city | Khlong Luang |
| Inspection start date | Sep 26, 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: