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Protalix Ltd — FDA Facility Profile

FEI 3008289067

Protalix Ltd is an FDA-registered facility (FEI 3008289067) located in Carmiel, IL. Registered operations: ANALYSIS; API MANUFACTURE; MANUFACTURE. RegDataLab tracks 4 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Jul 11, 2019: No Action Indicated (NAI)
Inspections on record
4 (2 VAI, 2 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

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
Jul 11, 2019No Action Indicated (NAI)No citations listed
May 14, 2015Voluntary Action Indicated (VAI)No citations listed
Nov 11, 2010No Action Indicated (NAI)No citations listed
Oct 17, 2010Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Protalix Ltd.
Location
Carmiel (IL)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; API MANUFACTURE; MANUFACTURE
Source
decrs

FDA data resources

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