Warning letter
Progressive Medical Inc: warning letter of Jan 10, 2012
FDA warning letter 252794 · Kansas City District Office
Key facts
| Reference number | 252794 |
|---|---|
| Company | Progressive Medical Inc |
| Subject | CGMP/QSR/Medical Devices/Adulterated/Misbranded |
| Issue date | Jan 10, 2012 |
| Posted date | Jan 10, 2012 |
| Issuing office | Kansas City District Office |
| Product type | Devices |
| CFR sections cited | 820, 803, 803.17, 820.40 |
| Inspection city | Fenton |
| Inspection ZIP | 63026 |
| Inspection start date | Aug 30, 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: