LAURUS LABS LIMITED — FDA Facility Profile

FEI 3007083664

LAURUS LABS LIMITED is an FDA-registered facility (FEI 3007083664) located in Anakapalli, IN. Registered operations: ANALYSIS; API MANUFACTURE. RegDataLab tracks 6 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Apr 19, 2024: No Action Indicated (NAI)
Inspections on record
6 (3 VAI, 3 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Import refusals
8

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 19, 2024No Action Indicated (NAI)No citations listed
Jun 14, 2019Voluntary Action Indicated (VAI)No citations listed
Aug 18, 2017Voluntary Action Indicated (VAI)No citations listed
Apr 24, 2015No Action Indicated (NAI)No citations listed
Nov 27, 2012Voluntary Action Indicated (VAI)No citations listed
Oct 29, 2009No Action Indicated (NAI)No citations listed

Facility details

Company
Laurus Labs Limited
Location
Anakapalli (IN)
Registration Expires
Dec 31, 2027
Operations
ANALYSIS; API MANUFACTURE
Source
decrs

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.