Warning letter
Simpro: warning letter of Aug 17, 2016
FDA warning letter 506504 · Dallas District Office
Key facts
| Reference number | 506504 |
|---|---|
| Company | Simpro |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Aug 17, 2016 |
| Posted date | Aug 30, 2016 |
| Issuing office | Dallas District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.17, 807.97, 820, 884.2660 |
| Inspection city | Irving |
| Inspection ZIP | 75063 |
| Inspection start date | Jun 17, 2016 |
| 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: