Centurion Labs, LLC
FDA Regulatory Profile
Centurion Labs, LLC has 2 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record.
- Latest recall
- D-1141-2017 · Class II · Aug 22, 2017
- Latest inspection
- May 14, 2025 · NAI
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 2 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 1 | 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 |
|---|
| D-1141-2017 | Class II | Ninjacof-A (Acetaminophen 160 mg, Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral… | Aug 22, 2017 |
| D-1140-2017 | Class II | Ninjacof (Chlophedianol HCL 12.5 mg and Pyrilamine Maleate 12.5 mg) Oral Solution, 16 fl. oz. (473… | Aug 22, 2017 |
Recent FDA Inspections
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.
Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 3007457365 | Hoover, AL | 1 | May 14, 2025 |