Warning letter
Pace Tech, Inc. [ARCHIVED]: warning letter of Nov 1, 2011
FDA warning letter 213474 · Florida District Office
Key facts
| Reference number | 213474 |
|---|---|
| Company | Pace Tech, Inc. [ARCHIVED] |
| Subject | CGMP/QSR/Medical Devices/Adulterated/Misbranded |
| Issue date | Nov 1, 2011 |
| Posted date | Nov 1, 2011 |
| Issuing office | Florida District Office |
| Product type | Devices |
| CFR sections cited | 803.17, 820, 803, 803.3, 803.22 |
| Inspection city | Clearwater |
| Inspection ZIP | 33756 |
| Inspection start date | Jul 7, 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: