Warning letter
Anybattery, Inc.: warning letter of Apr 29, 2015
FDA warning letter 447357 · Minneapolis District Office
Key facts
| Reference number | 447357 |
|---|---|
| Company | Anybattery, Inc. |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Apr 29, 2015 |
| Posted date | May 11, 2015 |
| Issuing office | Minneapolis District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.3, 803.17, 878.4820, 820, 803.50(a), 807.81(b) |
| Inspection city | Rosemount |
| Inspection ZIP | 55068 |
| Inspection start date | Oct 21, 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: