Inspection classificationInspection ended May 15, 2026

FDA inspection of Mylan Laboratories Limited: OAI

Official action indicated

FDA's record ↗

FDA classified an inspection of Mylan Laboratories Limited in Nashik, India as OAI (official action indicated). The inspection ended on May 15, 2026. Product type: Drugs.

On the record

Establishment
Mylan Laboratories Limited
Location
Nashik, India
Classification
OAI · Official action indicated
Inspection ended
2026-05-15
Product type
Drugs
Fiscal year
FY2026
FDA establishment identifier (FEI)
3005587313
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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