# Yichang Humanwell Oral Solid Dosage Plant – FDA Inspection, Jun 28, 2019

Source: https://www.keypedia.com/records/fda_inspections/yichang-humanwell-oral-solid-dosage-plant/e8869ffa-eeb1-4cfc-a810-53fc37918e93
Source feed: FDA_Inspections

> FDA inspection 1095074 of Yichang Humanwell Oral Solid Dosage Plant, June 28, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095074
- Company Name: Yichang Humanwell Oral Solid Dosage Plant
- Inspection Date: 2019-06-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

- [FDA Inspection 1215546 - 2023-07-21](https://www.keypedia.com/records/fda_inspections/yichang-humanwell-oral-solid-dosage-plant/f7f132d2-91d5-46b0-bb0e-77b079bde60d)
- FDA Inspection 1063246 - 2018-06-29
- FDA Inspection 1000211 - 2017-01-06

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/marcus-a-ray/d394d757-5569-4697-bec1-c24113e29d6f)

Company: https://www.keypedia.com/companies/yichang-humanwell-oral-solid-dosage-plant/5757d69c-083b-427c-8ee0-a2aa0b6b11c4

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c
