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Kevin Martin — FDA Facility Profile

FEI 3012788109

Kevin Martin is an FDA-inspected facility (FEI 3012788109) located in New Paris, IN, US. RegDataLab tracks 1 FDA inspection at this facility.

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What FDA found at this site

Latest inspection
Mar 24, 2017: Official Action Indicated (OAI)
Inspections on record
1 (1 OAI)
Last OAI inspection
Mar 24, 2017
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
Mar 24, 2017Official Action Indicated (OAI)Drugs prohibited for extralabel use in food-producing animal(s) (21 CFR 530.41(a))
ELDU - producer causes Illegal drug residue (21 CFR 530.11(d))
ELDU without veterinary client-patient relationship (FDCA 501(a)(5))
Record keeping (FDCA 402(a)(4))

Facility details

Company
Kevin Martin
Location
New Paris, IN (US)
Source
inspections

FDA data resources

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