CAMBREX PROFARMACO MILANO SRL — FDA Facility Profile

FEI 3003723076

CAMBREX PROFARMACO MILANO SRL is an FDA-registered facility (FEI 3003723076) located in MILANO, IT. Registered operations: ANALYSIS; API MANUFACTURE. RegDataLab tracks 8 FDA inspections and 1 compliance action at this facility.

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What FDA found at this site

Latest inspection
Nov 11, 2022: No Action Indicated (NAI)
Inspections on record
8 (1 OAI, 3 VAI, 4 NAI)
Last OAI inspection
Mar 31, 2009
Warning letters
1 listed by FDA for this FEI, latest Aug 12, 2009
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
Nov 11, 2022No Action Indicated (NAI)No citations listed
Oct 1, 2021Voluntary Action Indicated (VAI)No citations listed
May 7, 2019No Action Indicated (NAI)No citations listed
May 19, 2017Voluntary Action Indicated (VAI)No citations listed
Nov 6, 2015Voluntary Action Indicated (VAI)No citations listed
Dec 6, 2013No Action Indicated (NAI)No citations listed
Mar 25, 2011No Action Indicated (NAI)No citations listed
Mar 31, 2009Official Action Indicated (OAI)No citations listed

Facility details

Company
Cambrex Profarmaco Milano Srl
Location
MILANO (IT)
Registration Expires
Dec 31, 2027
Operations
ANALYSIS; API MANUFACTURE
Source
decrs

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