Warning letter
Electronic Development Labs, Inc: warning letter of Oct 1, 2014
FDA warning letter 423609 · Baltimore District Office
Key facts
| Reference number | 423609 |
|---|---|
| Company | Electronic Development Labs, Inc |
| Subject | Medical Device Reporting/Misbranded |
| Issue date | Oct 1, 2014 |
| Posted date | Nov 11, 2014 |
| Issuing office | Baltimore District Office |
| Product type | Devices |
| CFR sections cited | 803.17 |
| Inspection city | Danville |
| Inspection ZIP | 24540-7342 |
| Inspection start date | Oct 29, 2013 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- ADC 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: