Warning letter
Tiller MIND BODY, Inc.: warning letter of Feb 25, 2015
FDA warning letter 439175 · Dallas District Office
Key facts
| Reference number | 439175 |
|---|---|
| Company | Tiller MIND BODY, Inc. |
| Subject | Medical Device/Adulterated/Misbranded/Lacks PMA and/or 510(k) |
| Issue date | Feb 25, 2015 |
| Posted date | Mar 24, 2015 |
| Issuing office | Dallas District Office |
| Product type | Devices |
| CFR sections cited | 876.5220, 876.5220(b)(2), 876.5220(b)(1), 807.81(b), 820, 807.97, 807.81(a)(3)(ii) |
| Inspection city | San Antonio |
| Inspection ZIP | 78213 |
| Inspection start date | Jun 23, 2014 |
| 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: