OneSource Specialty Pharma Limited — Bengaluru
USFDA inspection record for FEI 3003813519, Bengaluru, India.
VAI
Latest classification
2
Inspections on record
3
Form 483 observations on record
History (newest first)
Inspections
30 Jun 2026
VAI — Voluntary action indicated
Drug Quality Assurance · Drugs · FY2026
Source: FDA Data Dashboard ↗
28 Mar 2024
VAI — Voluntary action indicated
Drug Quality Assurance · Drugs · FY2024
Form 483: 3 observations
- Failing drug products not rejected (21 CFR 211.165(f))
- Representative Samples (21 CFR 211.84(b))
- Record maintenance 1 year (except exempt OTC) (21 CFR 211.180(b))
Source: FDA Data Dashboard ↗
📎 Cite this data: Source: PharmaRoz, FDA inspection record for FEI 3003813519, updated 12 Nov 2026