Gilead Alberta ULC FDA Inspection Record

FEI 3001027806 ยท Inspections, Form 483s, warning letters and import refusals

Gilead Alberta ULC is an FDA-registered facility (FEI 3001027806) located in Edmonton, CA. 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
May 12, 2023: No Action Indicated (NAI)
Inspections on record
6 (6 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
1

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
May 12, 2023No Action Indicated (NAI)No citations listed
Jan 27, 2017No Action Indicated (NAI)No citations listed
Mar 7, 2014No Action Indicated (NAI)No citations listed
Oct 25, 2012No Action Indicated (NAI)No citations listed
Aug 5, 2011No Action Indicated (NAI)No citations listed
Mar 26, 2009No Action Indicated (NAI)No citations listed

Facility details

Company
Gilead Alberta ULC
Location
Edmonton (CA)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; API MANUFACTURE
Source
decrs

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