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Zolberg Corporation FDA Inspection Record

FEI 3004200690 · Inspections, Form 483s, warning letters and import refusals

Zolberg Corporation is an FDA-registered facility (FEI 3004200690) located in Philippines (PHL). Registered operations: MANUFACTURE. RegDataLab tracks 3 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Dec 7, 2023: Voluntary Action Indicated (VAI)
Inspections on record
3 (2 VAI, 1 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
3

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
Dec 7, 2023Voluntary Action Indicated (VAI)No citations listed
May 5, 2017Voluntary Action Indicated (VAI)No citations listed
Mar 23, 2012No Action Indicated (NAI)No citations listed

Facility details

Company
Zolberg Corporation
Location
Philippines (PHL)
Registration Expires
Dec 31, 2026
Operations
MANUFACTURE
Source
decrs

Import refusals

FDA data resources

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