Warning letter
W.H.P.M, Inc.: warning letter of Jun 30, 2022
FDA warning letter 629146 · Office of Medical Device and Radiological Health Division 3
Key facts
| Reference number | 629146 |
|---|---|
| Company | W.H.P.M, Inc. |
| Subject | Unapproved Products Related to the Coronavirus Disease 2019 (COVID-19) |
| Issue date | Jun 30, 2022 |
| Posted date | Jul 12, 2022 |
| Issuing office | Office of Medical Device and Radiological Health Division 3 |
| Product type | Devices |
| CFR sections cited | 820 |
| Inspection city | Irwindale |
| Inspection ZIP | 91706 |
| Inspection start date | Feb 7, 2022 |
| Letter on fda.gov | fda.gov |
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: