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EuropTec Polymer AG

FDA establishment 3010287665, Oftringen, Switzerland. Every inspection FDA has posted for the site, with its outcome and cited regulations.

  • Inspections: 1
  • Official action indicated: 0
  • Last inspection ended: Sep 25, 2025
  • Warning letters: 0

Inspections by Fiscal Year

FY2018 to FY2027 to date; 0 classified OAI

Most Cited at This Site

Inspections citing each reference

Inspections

1 inspections, newest first
EndedProduct and areaCitationsClassification
Sep 25, 2025Devices · Compliance: Devices
2 cited references
  • 21 CFR 820.186. QSR The quality system record has not been adequately maintained.
  • 21 CFR 820.90(a). Nonconforming product, Lack of or inadequate procedures Procedures have not been adequately established to control product that does not conform to specified requirements.
Voluntary Action Indicated (VAI)

Identifiers

FEI number
3010287665
FDA firm profile
Data Dashboard

An FEI (FDA Establishment Identifier) names one physical site. Inspections, outcomes and citations come from FDA's Data Dashboard; FDA posts citations only for some inspections. A contract site can make products for many companies, so the company shown is the one FDA lists as the site's firm. FDA Data Dashboard and warning letters

Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.