PRECISION FORMS, INC. FDA Inspection Record

FEI 3010041993 · Inspections, Form 483s, warning letters and import refusals

PRECISION FORMS, INC. is an FDA-registered facility (FEI 3010041993) located in Butler, NJ, US. RegDataLab tracks 5 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
May 1, 2025: No Action Indicated (NAI)
Inspections on record
5 (5 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
May 1, 2025No Action Indicated (NAI)Lack/Inad procedure-Monitoring/Control of Validated Proces (21 CFR 820.75(b))
Lack of or inadequate procedures (21 CFR 820.100(a))
Lack of or inadequate process validation (21 CFR 820.75(a))
Aug 31, 2022No Action Indicated (NAI)No citations listed
Dec 4, 2019No Action Indicated (NAI)No citations listed
Jan 20, 2016No Action Indicated (NAI)No citations listed
May 2, 2013No Action Indicated (NAI)No citations listed

Facility details

Company
Precision Forms, Inc.
Location
Butler, NJ (US)
Source
device

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