FDA Inspection 910769 — Raybow (Suzhou) Pharmaceutical Co., Ltd.

Raybow (Suzhou) Pharmaceutical Co., Ltd. — FEI 3007114474

The FDA completed an inspection of Raybow (Suzhou) Pharmaceutical Co., Ltd. on Sep 19, 2014 in Suzhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 19, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Suzhou (China)

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