Warning letter
James P. Johnston, CO, dba Midwest Ocular Prosthetics [ARCHIVED]: warning letter of Mar 17, 2010
FDA warning letter 82424 · Center for Devices and Radiological Health
Key facts
| Reference number | 82424 |
|---|---|
| Company | James P. Johnston, CO, dba Midwest Ocular Prosthetics [ARCHIVED] |
| Subject | Device/Misbranded, |
| Issue date | Mar 17, 2010 |
| Posted date | Mar 17, 2010 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| Inspection city | Michigan City |
| Inspection ZIP | 46360 |
| Inspection start date | May 1, 2009 |
| Letter on fda.gov | web.archive.org |
At a glance
- NAI Linked inspection classification
- No Form FDA 483 issued
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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: