Meril Endo Surgery Pvt. Ltd. — Pardi
USFDA inspection record for FEI 3007205024, Pardi, India.
VAI
Latest classification
1
Inspections on record
2
Form 483 observations on record
History (newest first)
Inspections
12 Jan 2023
VAI — Voluntary action indicated
Compliance: Devices · Devices · FY2023
Form 483: 2 observations
- DMR - not or inadequately maintained (21 CFR 820.181)
- Lack of or inadequate process validation (21 CFR 820.75(a))
Source: FDA Data Dashboard ↗
📎 Cite this data: Source: PharmaRoz, FDA inspection record for FEI 3007205024, updated 12 Nov 2026