Drug factory · FDA FEI 3012248027
Alvix Laboratories, LLC
Ocean Springs, Mississippi, United States
Matched to FDA's records by company name, because this plant's registration on the label has expired.
No problems found at FDA's last inspection, Sep 16, 2016.
No Action Indicated: inspectors found no objectionable conditions.
1 drug inspection on record since 2016: 1 with no problems, 0 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Lidocaine and Prilocaine | Makes it | Alvix Laboratories, LLC | 15455-9504 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Sep 16, 2016 | No problems found | Drug Quality Assurance | — |