Facility

Advanced Instruments, LLC

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

Key facts

2recalls · worst Class II

—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)	1221020
Establishment type	Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	25 BRADLEY DR. WESTBROOK, ME, US 04092
Registration status	Active · expires 2026
Parent company	ADVANCED INSTRUMENTS, LLC (owner-operator 1217058)
Brand names	Beckman Turbidity Meter

Activity by year

Recalls (2)

Devices registered here (1)

Colorimeter, Photometer, Spectrophotometer For Clinical Use
Product code JJQ (opens in a new tab) · Class I · Clinical Chemistry · 21 CFR 862.2300

Recalls & enforcement

Class IIOngoing2024-03-11
System error messages may delay the ability to test patient samples and the need for frequent calibration due to results outside the expected range when testing controls.
Class IITerminated2018-02-07
RBC Reagent failure. High fluorescent counts during RBC Reagent + Diluent QC check that will result in failed QC check, preventing user from testing patient samples for RBC.

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. “Advanced Instruments, LLC (FEI 1221020) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1221020-advanced-instruments-llc/

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