Keystone Industries

Gibbstown, United States keystoneindustries.com

Overview

Keystone Industries is a pharmaceutical company headquartered in Gibbstown, United States, founded in 1908, with 201-500 employees.

FDA compliance signals

34 FDA enforcement records linked to this company.

  • recall — Class II2026-06-24

    Defective container:may contain bottles with incomplete seals

  • recall — Class II2026-06-24

    Defective container:may contain bottles with incomplete seals

  • recall — Class II2026-06-24

    Defective container:may contain bottles with incomplete seals

  • recall — Class II2026-06-24

    Defective container:may contain bottles with incomplete seals

  • recall — Class II2026-06-24

    Defective container:may contain bottles with incomplete seals

  • recall — Class II2026-06-24

    Defective container:may contain bottles with incomplete seals

  • recall — Class II2026-06-24

    Defective container:may contain bottles with incomplete seals

  • 4832025-11-07

    Component identity verification

  • recall — Class II2024-12-25

    CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.

  • recall — Class II2024-12-25

    CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.

  • recall — Class II2024-12-25

    CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.

  • recall — Class II2024-12-25

    CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.

  • recall — Class II2024-12-25

    CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.

  • recall — Class II2024-12-25

    CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.

  • recall — Class II2024-12-25

    CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.

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