Warning letter
Folsum Metal Products, Inc. dba FRONTIER DEVICES [ARCHIVED]: warning letter of Aug 27, 2009
FDA warning letter 58382 · New Orleans District Office
Key facts
| Reference number | 58382 |
|---|---|
| Company | Folsum Metal Products, Inc. dba FRONTIER DEVICES [ARCHIVED] |
| Subject | CGMP/QSR/Manufacture/Packing/Storage/Installation/Adulterated |
| Issue date | Aug 27, 2009 |
| Posted date | Aug 27, 2009 |
| Issuing office | New Orleans District Office |
| Product type | Devices |
| CFR sections cited | 820, 803, 803.11, 803.12, 803.50(a)(1), 803.50(a)(2), 803.50(b)(3) |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
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: