FDA Device Entity Profile: FERNO-WASHINGTON, INC.

Known Identifiers & Locations

FEI Numbers 1523574, 3003122141, 3004755235, 3005772723

Owner Operator Numbers 10025359, 1523574

Locations Covered Oakville Ontario, CA; Pieve di Centa, BO Prato, IT; Slovak Republic Trenciansky, SK; Wilmington, OH, US

Registered Establishments (4)

Registration #	Establishment Name	Location	Establishment Type(s)	Action
1523574	FERNO-WASHINGTON, INC.	Wilmington, OH, US	Complaint File Establishment per 21 CFR 820.198,Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device	View Details
3004755235	Ferno Slovakia s.r.o.	Slovak Republic Trenciansky, SK	Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device	View Details
3005772723	Traverse Rescue LLC	Oakville Ontario, CA	Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device	View Details
9617285	FERNO S.R.L.	Pieve di Centa, BO Prato, IT	Complaint File Establishment per 21 CFR 820.198,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.

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