FDA Inspection 1084134 — Henan Kangdi Medical Devices Co. Ltd
The FDA completed an inspection of Henan Kangdi Medical Devices Co. Ltd on March 7, 2019 in Zhoukou. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- March 7, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Zhoukou (China)