Key Event and Dates
- The United States Food and Drug Administration (USFDA) conducted an inspection at the company's manufacturing facility located at Pashamylaram, Hyderabad (FEI No. 1000623515).
- The company had previously communicated about this inspection on 5 August 2026.
- On 7 November 2026, the company disclosed that USFDA has issued the Establishment Inspection Report (EIR) for this facility.
- The inspection has been classified by USFDA as Voluntary Action Indicated (VAI).
- With the receipt of the EIR, the inspection stands concluded.
Facility Details
The facility subject to inspection is located at Pashamylaram, Hyderabad and has FEI (Facility Establishment Identifier) Number 1000623515.