Warning letter
Innovative Products Unlimited, Inc.: warning letter of Mar 4, 2003
FDA warning letter UCM147346 · Detroit District Office
Key facts
| Reference number | UCM147346 |
|---|---|
| Company | Innovative Products Unlimited, Inc. |
| Subject | Medical Device Reporting Regulations/Quality System Regulation/Adulterated/Misbranded |
| Issue date | Mar 4, 2003 |
| Posted date | Mar 4, 2003 |
| Issuing office | Detroit District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.50, 820, 820.40 |
| Country | 3 |
| Inspection city | Niles |
| Inspection ZIP | 49120-1233 |
| Inspection start date | May 28, 2002 |
| 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: