Vitalabs, Inc.
FDA Regulatory Profile
Vitalabs, Inc. has 1 FDA recall, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest recall
- H-0037-2026 · Class II · Jun 13, 2025
- Latest inspection
- Sep 28, 2023 · VAI
Reviewing Vitalabs, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.
Check this supplier
Or check Vitalabs, Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.
Get a free API key
Is this your company or a supplier you list? Link to this FDA record from your site with a free button.
Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
| Recalls | 1 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 6 | Nov 11, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
Recent Recalls
| Number | Class | Product | Date |
| H-0037-2026 | Class II | vitamins B12 dietary supplement Raspberry Flavored sold under the following brand names: 1. Black… | Jun 13, 2025 |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
| Sep 28, 2023 | McDonough, GA | Food/Cosmetics | Voluntary Action Indicated (VAI) | 1048033 |
| Jun 29, 2022 | McDonough, GA | Food/Cosmetics | No Action Indicated (NAI) | 1048033 |
| Dec 19, 2018 | McDonough, GA | Food/Cosmetics | No Action Indicated (NAI) | 1048033 |
| Dec 1, 2016 | McDonough, GA | Food/Cosmetics | No Action Indicated (NAI) | 1048033 |
| Aug 2, 2016 | McDonough, GA | Food/Cosmetics | No Action Indicated (NAI) | 1048033 |
| Feb 21, 2014 | McDonough, GA | Food/Cosmetics | Voluntary Action Indicated (VAI) | 1048033 |
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
| FEI 1048033 | McDonough, GA | 6 | Sep 28, 2023 |