ONESOURCE SPECIALTY PHARMA LIMITED — Bengaluru
USFDA inspection record for FEI 3017501030, Bengaluru, India.
VAI
Latest classification
2
Inspections on record
3
Form 483 observations on record
History (newest first)
Inspections
28 Mar 2025
VAI — Voluntary action indicated
Drug Quality Assurance · Drugs · FY2025
Source: FDA Data Dashboard ↗
01 Sep 2022
VAI — Voluntary action indicated
Compliance: Devices · Devices · FY2022
Form 483: 3 observations
- Documentation (21 CFR 820.100(b))
- Quality System Procedures (21 CFR 820.20(e))
- Lack of or inadequate procedures (21 CFR 820.100(a))
Source: FDA Data Dashboard ↗
📎 Cite this data: Source: PharmaRoz, FDA inspection record for FEI 3017501030, updated 12 Nov 2026