Warning letter
Alma Lasers, Inc.: warning letter of Jun 7, 2013
FDA warning letter 394413 · Chicago District Office
Key facts
| Reference number | 394413 |
|---|---|
| Company | Alma Lasers, Inc. |
| Subject | Medical Device Reporting/Misbranded |
| Issue date | Jun 7, 2013 |
| Posted date | Jun 7, 2013 |
| Issuing office | Chicago District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.3, 803.17, 803.50(a)(1), 820, 820.3, 803.50(b) |
| Inspection city | Buffalo Grove |
| Inspection ZIP | 60089 |
| Inspection start date | Jan 17, 2013 |
| 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: