Facility

K&R TECHNOLOGIES DBA MICROBIOLOGY INTERNATIONAL

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

Key facts

1recalls · 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)	3013823481
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	5350 Partners Ct Frederick, MD, US 21703
Registration status	Active · expires 2026
Parent company	K&R Technologies dba Microbiology International (owner-operator 10091040)
Brand names	Whitley AtmoGen Jar Gassing System

Activity by year

Recalls (1)

Devices registered here (1)

Device, Gas Generating
Product code KZJ (opens in a new tab) · Class I · Microbiology · 21 CFR 866.2580

Recalls & enforcement

Class IIOngoing2024-12-02
Software defect concerning autosave mechanism may result in the clinician administering incorrect medication(s).

All facilities operated by K&R Technologies dba Microbiology International

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. “K&R TECHNOLOGIES DBA MICROBIOLOGY INTERNATIONAL (FEI 3013823481) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3013823481-k-r-technologies-dba-microbiology-intern/

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