Drug factory · FDA FEI 3002518976
S.A.L.A.R.S. SOCIETà AZIONARIA LABORATORI ALCALOIDI RIFORNIMENTI SANITARI S.P.A.
VIA SAN FRANCESCO D'ASSISI 5, Como (camerlata), Italy
Problems found, fixed voluntarily at FDA's last inspection, Sep 30, 2022.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
3 drug inspections on record since 2014: 0 with no problems, 3 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Naltrexone and Triamcinolone | Makes the active ingredient | Complete Pharmacy and Medical Solutions | 69364-3143 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Sep 30, 2022 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Jul 27, 2018 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Dec 12, 2014 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
Registered with FDA for: api manufacture.