FDA Inspection 1013794 — Symbiotec Pharmalab Limited

Symbiotec Pharmalab Limited — FEI 3009298759

The FDA completed an inspection of Symbiotec Pharmalab Limited on May 5, 2017 in Pithampur, Dhar. 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
May 5, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pithampur, Dhar (India)

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