Nippon Sanso Matheson, Inc. — FDA Facility Profile

FEI 3003730218

Nippon Sanso Matheson, Inc. is an FDA-registered facility (FEI 3003730218) located in Richmond, CA, US. Registered operations: MANUFACTURE. RegDataLab tracks 4 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Dec 19, 2019: Voluntary Action Indicated (VAI)
Inspections on record
4 (2 VAI, 2 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
Dec 19, 2019Voluntary Action Indicated (VAI)Complete test data included in records (21 CFR 211.194(a))
Aug 27, 2014No Action Indicated (NAI)No citations listed
Mar 30, 2011No Action Indicated (NAI)No citations listed
Jun 10, 2010Voluntary Action Indicated (VAI)Cleaning / Sanitizing / Maintenance (21 CFR 211.67(a))
Establish reliability of supplier's C of A (21 CFR 211.84(d)(2))
Records not made readily available to FDA (21 CFR 211.180(c))
Prepared for each batch, include complete information (21 CFR 211.188)
and 4 more

Facility details

Company
Nippon Sanso Matheson, Inc.
Location
Richmond, CA (US)
Registration Expires
Dec 31, 2027
Operations
MANUFACTURE
Source
decrs

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