Facility

LW SCIENTIFIC, INC.

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

Key facts

1recalls · worst Class II

2inspections · worst VAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3000251573
Establishment type	Repack or Relabel Medical Device
Location	865 Marathon Pkwy LAWRENCEVILLE, GA, US 30046
Registration status	Active · expires 2026
Parent company	LW SCIENTIFIC, INC. (owner-operator 9049895)

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (1)

Hemocytometer
Product code GHO (opens in a new tab) · Class I · Hematology · 21 CFR 864.6160

Recalls & enforcement

Class IITerminated2019-02-06
The clear, plastic, polycarbonate hematocrit rotor may break apart during use and be ejected through the plastic housing, posing a safety hazard to the technician and potentially damaging the surrounding area.

FDA inspections (2)

NAI2026-04-23
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
VAI2021-10-19
Voluntary Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

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.

All facilities operated by LW SCIENTIFIC, INC.

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. “LW SCIENTIFIC, INC. (FEI 3000251573) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3000251573-lw-scientific-inc/

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