Warning letter
In Vivo Metric Systems Corporation: warning letter of Mar 17, 2006
FDA warning letter UCM075833 · San Francisco District Office
Key facts
| Reference number | UCM075833 |
|---|---|
| Company | In Vivo Metric Systems Corporation |
| Subject | GMP Requirement/Quality System Regulations/Medical Device Reporting |
| Issue date | Mar 17, 2006 |
| Posted date | Mar 17, 2006 |
| Issuing office | San Francisco District Office |
| Product type | Devices |
| CFR sections cited | 898.12(a), 803, 830, 820, 898 |
| Country | 3 |
| Inspection city | Healdsburg |
| Inspection ZIP | 95448-4700 |
| Inspection start date | Sep 13, 2005 |
| 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: