Warning letter
Christus Spohn Hospital Corpus Christi - Memorial Campus [ARCHIVED]: warning letter of May 5, 2011
FDA warning letter 175392 · Center for Devices and Radiological Health
Key facts
| Reference number | 175392 |
|---|---|
| Company | Christus Spohn Hospital Corpus Christi - Memorial Campus [ARCHIVED] |
| Subject | Institutional Review Board (IRB) |
| Issue date | May 5, 2011 |
| Posted date | May 5, 2011 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 56.107(e), 56.115(a)(2), 56.108(c) |
| Inspection city | Corpus Christi |
| Inspection ZIP | 78405 |
| Inspection start date | Jan 28, 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: