Warning letter
Healthline Medical Products Inc: warning letter of May 31, 2007
FDA warning letter UCM076404 · Florida District Office
Key facts
| Reference number | UCM076404 |
|---|---|
| Company | Healthline Medical Products Inc |
| Subject | CGMP for Medical Devices/QSR/Adulterated/Misbranded |
| Issue date | May 31, 2007 |
| Posted date | May 31, 2007 |
| Issuing office | Florida District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.17, 803.50(a)(1) |
| Country | 3 |
| Inspection city | Winter Garden |
| Inspection ZIP | 34787-3732 |
| Inspection start date | Feb 13, 2007 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- VAI 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: