MEGHMANI LLP — Dahej
USFDA inspection record for FEI 3030599291, Dahej, India.
VAI
Latest classification
1
Inspections on record
3
Form 483 observations on record
History (newest first)
Inspections
03 Feb 2026
VAI — Voluntary action indicated
Drug Quality Assurance · Drugs · FY2026
Form 483: 3 observations
- Rejected Material Area (21 CFR 211.42(c)(2))
- Identification of containers, lines, equipment (21 CFR 211.105(a))
- Drug product sample (21 CFR 211.160(b)(3))
Source: FDA Data Dashboard ↗
📎 Cite this data: Source: PharmaRoz, FDA inspection record for FEI 3030599291, updated 12 Nov 2026