Inspection classificationInspection ended June 30, 2026

FDA inspection of OneSource Specialty Pharma Limited: VAI

Voluntary action indicated

FDA's record ↗

FDA classified an inspection of OneSource Specialty Pharma Limited in Bengaluru, India as VAI (voluntary action indicated). The inspection ended on June 30, 2026. Product type: Drugs.

On the record

Establishment
OneSource Specialty Pharma Limited
Location
Bengaluru, India
Classification
VAI · Voluntary action indicated
Inspection ended
2026-06-30
Product type
Drugs
Fiscal year
FY2026
FDA establishment identifier (FEI)
3003813519
Source
FDA Data Dashboard ↗

The full record

An account shows the project areas inspected and whether citations were posted.

What an inspection classification is

After an inspection FDA classifies the outcome. NAI (no action indicated): no objectionable conditions were found, or none that justify further action. VAI (voluntary action indicated): objectionable conditions were found, but the agency is not prepared to take or recommend regulatory action. OAI (official action indicated): regulatory or administrative action is recommended.

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From FDA Data Dashboard; FDA posts a classification after its review, which can be months after the inspection ended. The record may have changed since it was read.

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