FDA Inspection 1050171 — NINGBO HECAI MEDICAL EQUIPMENT CO. LTD.
The FDA completed an inspection of NINGBO HECAI MEDICAL EQUIPMENT CO. LTD. on Apr 5, 2018 in Ningbo. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Apr 5, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Ningbo (China)