Facility

QUANTIMETRIX CORP.

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

Key facts

1recalls · worst Class III

—inspections in our data

—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)	2020715
Establishment type	Manufacture Medical Device
Location	2005 Manhattan Beach Blvd REDONDO BEACH, CA, US 90278
Registration status	Active · expires 2026
Parent company	QUANTIMETRIX CORP. (owner-operator 2020715)
Brand names	Sweat Control for Cystic Fibrosis Testing

Activity by year

Recalls (1)

Devices registered here (1)

Electrolyte Controls (Assayed And Unassayed)
Product code JJR (opens in a new tab) · Class I · Clinical Chemistry · 21 CFR 862.1660

Recalls & enforcement

Class IIITerminated2017-12-21
The kits contained an incorrect lot of Dropper Plus Level 1 vials

All facilities operated by QUANTIMETRIX CORP.

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. “QUANTIMETRIX CORP. (FEI 2020715) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/2020715-quantimetrix-corp/

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