Warning letter
Shima Laboratories Co., Ltd.: warning letter of Mar 21, 2014
FDA warning letter 418378 · Center for Devices and Radiological Health
Key facts
| Reference number | 418378 |
|---|---|
| Company | Shima Laboratories Co., Ltd. |
| Subject | CGMP/QSR/Manufacture/Packing/Storage/Installation/Adulterated |
| Issue date | Mar 21, 2014 |
| Posted date | May 5, 2014 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 803.50(b), 803, 803.50(a), 803.17, 820, 803.3 |
| Inspection city | Itabashi |
| Inspection start date | Sep 30, 2013 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- 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: