Warning letter
Mayer Laboratories, Inc. [ARCHIVED]: warning letter of Jul 5, 2011
FDA warning letter 167292 · San Francisco District Office
Key facts
| Reference number | 167292 |
|---|---|
| Company | Mayer Laboratories, Inc. [ARCHIVED] |
| Subject | Lacks Premarket Approval Application/Adulterated/Misbranded |
| Issue date | Jul 5, 2011 |
| Posted date | Jul 5, 2011 |
| Issuing office | San Francisco District Office |
| Product type | Devices |
| CFR sections cited | 807.81(b), 807.81(a)(3)(i), 807.100(a) |
| Inspection city | Berkeley |
| Inspection ZIP | 94704 |
| Inspection start date | Jan 24, 2011 |
| 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: