Warning letter
Swedish Bitters Herbs Company [ARCHIVED]: warning letter of Nov 8, 2010
FDA warning letter 126230 · Kansas City District Office
Key facts
| Reference number | 126230 |
|---|---|
| Company | Swedish Bitters Herbs Company [ARCHIVED] |
| Subject | CGMP For Manufacturing, Packing, Labeling, or Holding for Dietary Supplements/Adulterated |
| Issue date | Nov 8, 2010 |
| Posted date | Nov 8, 2010 |
| Issuing office | Kansas City District Office |
| Product type | Food/Cosmetics |
| CFR sections cited | 101.36, 111, 111.73, 111.103, 111.27(d), 111.35(b)(1)(iii), 111.205(a), 111.255(a), 101.36(b)(2)(i), 101.36(c)(3), 111.75(a)(1), 111.75(a)(1)(i) and 3 more |
| Inspection city | Concordia |
| Inspection ZIP | 64020 |
| Inspection start date | Jul 6, 2010 |
| 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: