FDA Inspection 1028538 — Glenmark Pharmaceuticals Limited

Glenmark Pharmaceuticals Limited — FEI 3008565058

The FDA completed an inspection of Glenmark Pharmaceuticals Limited on Aug 26, 2017 in Dhar. 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
Aug 26, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dhar (India)

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