FDA Inspection 980987 — Qilu SYNVA Pharmaceutical Co. Ltd

Qilu SYNVA Pharmaceutical Co. Ltd — FEI 3006385404

The FDA completed an inspection of Qilu SYNVA Pharmaceutical Co. Ltd on Jun 17, 2016 in Dezhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 17, 2016
Fiscal Year
2016
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Dezhou (China)

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