# Joyang Laboratories – FDA Inspection, May 5, 2017

Source: https://www.keypedia.com/records/fda_inspections/joyang-laboratories/ba24452a-e8bc-4f52-88f5-faa9caf0baf2
Source feed: FDA_Inspections

> FDA inspection 1021129 of Joyang Laboratories, May 05, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1021129
- Company Name: Joyang Laboratories
- Inspection Date: 2017-05-05
- 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 1268707 - 2025-04-25](https://www.keypedia.com/records/fda_inspections/joyang-laboratories/02fd8730-75bb-4da7-9b52-484e0d59fd05)
- FDA Inspection 1135083 - 2019-08-22

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/latorie-s-jones/086d0897-7d63-4fa8-bdce-f1d17885abd7)

Company: https://www.keypedia.com/companies/joyang-laboratories/4c659fb4-d8af-40f9-8426-507ab453e179

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