Drug factory · FDA FEI 1000150204
Air Source Industries
3976 Cherry Avenue, Long Beach, CA, United States
Problems found, fixed voluntarily at FDA's last inspection, Nov 15, 2017.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
1 drug inspection on record since 2017: 0 with no problems, 1 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Carbon Dioxide | Makes it | Air Source Industries Inc | 10167-500 |
| Helium | Makes it | Air Source Industries Inc | 10167-300 |
| Nitrogen | Makes it | Air Source Industries Inc | 10167-400 |
| Nitrous Oxide | Makes it | Air Source Industries Inc | 10167-200 |
| Oxygen | Makes it | Air Source Industries Inc | 10167-100, 10167-600 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Nov 15, 2017 | 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.
Nov 15, 2017 inspection
- Records reviewed annually 21 CFR 211.180(e)
Records are not maintained so that data therein can be reviewed at least annually to evaluate the quality standards of each drug product to determine the need for changes in specifications or manufacturing or control procedures.
Registered with FDA for: manufacture.