Warning letter
Global Protection Corp.: warning letter of Jan 7, 2008
FDA warning letter UCM1048449 · New England District Office
Key facts
| Reference number | UCM1048449 |
|---|---|
| Company | Global Protection Corp. |
| Subject | CGMP/QSR/Medical Device Reporting/Adulterated |
| Issue date | Jan 7, 2008 |
| Posted date | Jan 7, 2008 |
| Issuing office | New England District Office |
| Product type | Devices |
| CFR sections cited | 820 |
| Country | 3 |
| Inspection city | Boston |
| Inspection ZIP | 02210-2323 |
| Inspection start date | Oct 31, 2007 |
| 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: