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Macfarlan Smith Limited — FDA Facility Profile

FEI 3002807530

Macfarlan Smith Limited is an FDA-registered facility (FEI 3002807530) located in Midlothian, GB. Registered operations: API MANUFACTURE. RegDataLab tracks 4 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Nov 29, 2021: Voluntary Action Indicated (VAI)
Inspections on record
4 (4 VAI)
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
7

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
Nov 29, 2021Voluntary Action Indicated (VAI)No citations listed
Nov 10, 2017Voluntary Action Indicated (VAI)No citations listed
Sep 4, 2015Voluntary Action Indicated (VAI)No citations listed
Apr 13, 2012Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Macfarlan Smith Limited
Location
Midlothian (GB)
Registration Expires
Dec 31, 2027
Operations
API MANUFACTURE
Source
decrs

Import refusals

FDA data resources

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