Drug factory · FDA FEI 3006689272
Anshi Pharmaceutical (Zhongshan) Inc.
Zhongshan, China
Matched to FDA's records by company name, because this plant's registration on the label has expired.
Problems found, fixed voluntarily at FDA's last inspection, Oct 27, 2017.
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 2012: 1 with no problems, 2 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Benzonatate | Makes it | AiPing Pharmaceutical, Inc. | 11788-027, 11788-028, 11788-029 |
| Folic Acid | Makes it | AiPing Pharmaceutical, Inc. | 11788-001 |
| Ibuprofen | Makes it | AiPing Pharmaceutical, Inc. | 11788-008, 11788-009, 11788-010 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Oct 27, 2017 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Mar 20, 2015 | No problems found | Drug Quality Assurance | — |
| Oct 31, 2012 | Problems found, fixed voluntarily | Drug Quality Assurance | — |