Facility

NOA MEDICAL INDUSTRIES

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

Key facts

1recalls · worst Class II

1inspections · 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)	1000118429
Establishment type	Manufacture Medical Device
Location	801 Terry Ln WASHINGTON, MO, US 63090
Registration status	Active · expires 2026
Parent company	Hoffmann NOA Medical Industries, LLC (owner-operator 10082335)
Brand names	Bariatric

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Bariatric Bed
Product code OSI (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5100

Recalls & enforcement

Class IIOngoing2024-11-05
Red button used to engage side rails can break or become stuck making it difficult to engage the side rail.

FDA inspections (1)

VAI2024-10-10
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 Hoffmann NOA Medical Industries, LLC

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. “NOA MEDICAL INDUSTRIES (FEI 1000118429) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000118429-noa-medical-industries/

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