Warning letter
Glottal Enterprises Inc.: warning letter of Apr 23, 2013
FDA warning letter 380560 · New York District Office
Key facts
| Reference number | 380560 |
|---|---|
| Company | Glottal Enterprises Inc. |
| Subject | Medical Device Reporting/Misbranded |
| Issue date | Apr 23, 2013 |
| Posted date | Apr 23, 2013 |
| Issuing office | New York District Office |
| Product type | Devices |
| CFR sections cited | 803.17, 820, 807.81(b), 803 |
| Inspection city | Syracuse |
| Inspection ZIP | 13210 |
| Inspection start date | Oct 9, 2012 |
| 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: