Warning letter
Multidata Systems International Corporation: warning letter of Dec 18, 2001
FDA warning letter UCM178273 · Center for Devices and Radiological Health
Key facts
| Reference number | UCM178273 |
|---|---|
| Company | Multidata Systems International Corporation |
| Subject | Electronic Product Radiation Control/Premarket Notification Requirements/Adulterated/Misbranded |
| Issue date | Dec 18, 2001 |
| Posted date | Dec 18, 2001 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 1040.10(h), 1040.10(g)(5), 807, 1002, 1003.21, 1003.30, 1004.1, 1004.2, 1010.2, 1003.10(b), 1003.11(c), 1040.10(g) |
| Country | 3 |
| Inspection city | Saint Louis |
| Inspection ZIP | 63132-1104 |
| Inspection start date | May 31, 2001 |
| 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: