Drug factory · FDA FEI 3003589213
Metz Medical, Inc
Kenosha, Wisconsin, 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, Nov 14, 2014.
No Action Indicated: inspectors found no objectionable conditions.
2 drug inspections on record since 2012: 1 with no problems, 1 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Oxygen | Repackages it | Metz Medical, Inc | 66767-998 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Nov 14, 2014 | No problems found | Drug Quality Assurance | — |
| Aug 13, 2012 | Problems found, fixed voluntarily | Drug Quality Assurance | 1 |
What inspectors wrote down
From FDA's Form 483 citations: conditions an investigator observed that may violate drug manufacturing rules, as FDA published them.
Aug 13, 2012 inspection
- Training , Education , Experience overall 21 CFR 211.25(a)
Employees engaged in the packing of a drug product lack the training required to perform their assigned functions.