FDA Inspection 1002295 — Nippon Sanso Matheson, Inc.

Nippon Sanso Matheson, Inc. — FEI 3019318

The FDA completed an inspection of Nippon Sanso Matheson, Inc. on Feb 10, 2017 in Albany, OR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 10, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Albany, OR (United States)

Citations

IDCFRDescription
113421 CFR 211.25(b)Supervisor Training/Education/Experience
201121 CFR 211.188(a)Accurate reproduction
356521 CFR 211.58Buildings not maintained in good state of repair

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