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Daniel Lautner — FDA Facility Profile

FEI 3013141740

Daniel Lautner is an FDA-inspected facility (FEI 3013141740) located in Evanston, IN, US. RegDataLab tracks 1 FDA inspection at this facility.

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What FDA found at this site

Latest inspection
Jul 13, 2017: Voluntary Action Indicated (VAI)
Inspections on record
1 (1 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

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 13, 2017Voluntary Action Indicated (VAI)Expired drugs administered (FDCA 501(a)(5))
Prescribed ELDU - vet causes an illegal drug residue (21 CFR 530.20(a)(2)(iv))
Record keeping (FDCA 402(a)(4))

Facility details

Company
Daniel Lautner
Location
Evanston, IN (US)
Source
inspections

FDA data resources

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