Warning letter
Revival Products, Inc.: warning letter of Aug 14, 2020
FDA warning letter 606640 · Office of Human and Animal Food Operations – East Division 3
Key facts
| Reference number | 606640 |
|---|---|
| Company | Revival Products, Inc. |
| Subject | CGMP/Dietary Supplement/Adulterated/Misbranded |
| Issue date | Aug 14, 2020 |
| Posted date | Sep 1, 2020 |
| Issuing office | Office of Human and Animal Food Operations – East Division 3 |
| Product type | Food/Cosmetics |
| CFR sections cited | 111.535(b), 111.570(b), 111.570(b)(2), 101, 101.4, 101.36, 111, 111.510, 111.530, 101.3(d), 111.14(b)(2), 111.127(h) and 5 more |
| Inspection city | Kernersville |
| Inspection ZIP | 27284 |
| Inspection start date | Feb 10, 2020 |
| Letter on fda.gov | fda.gov |
At a glance
- 10–99 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: