Warning letter
Induction Therapies, LLC: warning letter of Nov 23, 2021
FDA warning letter 616487 · Center for Devices and Radiological Health
Key facts
| Reference number | 616487 |
|---|---|
| Company | Induction Therapies, LLC |
| Subject | Investigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated Device |
| Issue date | Nov 23, 2021 |
| Posted date | Dec 7, 2021 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| Inspection city | Louisville |
| Inspection ZIP | 40223 |
| Inspection start date | Jun 15, 2021 |
| Letter on fda.gov | fda.gov |
At a glance
- 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: