FDA Device Entity Profile: WALMART INC.

Known Identifiers & Locations

FEI Numbers 2316750, 3003512352, 3005890070, 3010119835

Owner Operator Numbers 2316750

Locations Covered BENTONVILLE, AR, US; Crawfordsville, IN, US; Dallas, TX, US; Fayetteville, AR, US

Registered Establishments (4)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
2316750	WALMART INC.	BENTONVILLE, AR, US	Manufacture Medical Device	View Details
3003512352	Wal-Mart Optical Lab	Fayetteville, AR, US	Repack or Relabel Medical Device,Manufacture Medical Device	View Details
3005890070	Walmart Optical Lab	Dallas, TX, US	Repack or Relabel Medical Device,Manufacture Medical Device	View Details
3010119835	Wal-Mart Optical Lab #9065	Crawfordsville, IN, US	Repack or Relabel Medical Device,Manufacture Medical Device	View Details

510(k) Premarket Notifications (0)

No 510(k) notifications found for this entity.

FDA Recall History (0)

No recall records found for this entity.

Profile Disclaimer

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