RegWardenFDA facility compliance records
Facility

COOK VANDERGRIFT INC.

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2016: 1 inspections; 2018: 1 inspections; 2023: 1 recalls12016201712018201920202021202212023202420252026
  • Recalls (1)
  • Inspections (2)

Devices registered here (1)

  • Microtools, Assisted Reproduction (Pipettes)
    Product code MQH (opens in a new tab) · Class II · Obstetrics/Gynecology · 21 CFR 884.6130

Recalls & enforcement

FDA inspections (2)

  • NAI2018-09-12
    No Action Indicated · Compliance: Devices
  • NAI2016-10-21
    No Action Indicated · Compliance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “COOK VANDERGRIFT INC. (FEI 2522007) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2522007-cook-vandergrift-inc/

Not open yet

Alerts for COOK VANDERGRIFT INC.

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.