Warning letter
Estill Medical Technologies, Inc.: warning letter of Aug 23, 2005
FDA warning letter UCM075532 · Dallas District Office
Key facts
| Reference number | UCM075532 |
|---|---|
| Company | Estill Medical Technologies, Inc. |
| Subject | Current Good Manufacturing Practice Regulation/Adulterated |
| Issue date | Aug 23, 2005 |
| Posted date | Aug 23, 2005 |
| Issuing office | Dallas District Office |
| Product type | Unknown |
| CFR sections cited | 820 |
| Country | 3 |
| Inspection city | Arlington |
| Inspection ZIP | 76011-4726 |
| Inspection start date | Jul 5, 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: