FDA Inspection 884273 — Kekule Pharma Limited

Kekule Pharma Limited — FEI 3009261338

The FDA completed an inspection of Kekule Pharma Limited on Jun 13, 2014 in Jinnaram. 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
Jun 13, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jinnaram (India)

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