Home / Facilities / 3009797745

PT. Marizarasa Sarimurni — FDA Facility Profile

FEI 3009797745

PT. Marizarasa Sarimurni is an FDA-inspected facility (FEI 3009797745) located in Serang-Banten, ID. RegDataLab tracks 1 FDA inspection at this facility.

Reviewing PT. Marizarasa Sarimurni as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check PT. Marizarasa Sarimurni yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

What FDA found at this site

Latest inspection
Aug 25, 2015: Official Action Indicated (OAI)
Inspections on record
1 (1 OAI)
Last OAI inspection
Aug 25, 2015
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Import refusals
4

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
Aug 25, 2015Official Action Indicated (OAI)No citations listed

Facility details

Company
PT. Marizarasa Sarimurni
Location
Serang-Banten (ID)
Source
inspections

Import refusals

FDA data resources

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