PHARMASTER + FDA Inspection Record

FEI 3006627937 · Inspections, Form 483s, warning letters and import refusals

PHARMASTER + is an FDA-registered facility (FEI 3006627937) located in GRAND EST, FR. Registered operations: MANUFACTURE. RegDataLab tracks 1 FDA inspection at this facility.

Reviewing PHARMASTER + 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 PHARMASTER + 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
Apr 28, 2023: 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
Import refusals
8

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
Apr 28, 2023Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Pharmaster +
Location
GRAND EST (FR)
Registration Expires
Dec 31, 2026
Operations
MANUFACTURE
Source
decrs

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