Warning letter
JFD Enterprises Inc [ARCHIVED]: warning letter of Dec 14, 2009
FDA warning letter 76554 · Baltimore District Office
Key facts
| Reference number | 76554 |
|---|---|
| Company | JFD Enterprises Inc [ARCHIVED] |
| Subject | CGMP Regulation For Food/Adulterated |
| Issue date | Dec 14, 2009 |
| Posted date | Dec 14, 2009 |
| Issuing office | Baltimore District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 110.40(a), 101, 101.3, 101.4, 110, 101.5(a), 110.20(b)(1), 110.20(b)(7), 110.35(c), 110.35(d), 110.80(a)(7), 110.80(b)(1) |
| Inspection city | Baltimore |
| Inspection ZIP | 21224 |
| Inspection start date | Jul 15, 2009 |
| Letter on fda.gov | web.archive.org |
At a glance
- 10–99 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: