FDA Inspection 1299814 — Henan Enokon Medical Instrument Co., Ltd.

Henan Enokon Medical Instrument Co., Ltd. — FEI 3027553696

The FDA completed an inspection of Henan Enokon Medical Instrument Co., Ltd. on Jan 23, 2026 in Xinxiang. 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: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 23, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Xinxiang (China)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.