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FDA Inspection 1053522 — Vynacron Dental Resins, Inc.

Vynacron Dental Resins, Inc. — FEI 2242866

The FDA completed an inspection of Vynacron Dental Resins, Inc. on May 16, 2018 in Jackson, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 16, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Jackson, NJ (United States)

Facility

Other inspections at this facility

  • 1259194 (OAI Tue Jan 21 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1179084 (NAI Fri Aug 26 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 901251 (VAI Wed Oct 29 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 755049 (NAI Thu Dec 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources