DashboardForm 483sForm 483 Details

Elos Medtech Timmersdala AB Form 483 Details

Form 483
View FDA's record for this firm
Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3003847101.

Elos Medtech Timmersdala AB

Timmersdala, -, Sweden
Issue DateOctober 14, 2010
FEI Number3003847101
CountrySweden
Status
No Warning Letter
Product Type
Devices
Elos Medtech Timmersdala AB FDA Form 483, Timmersdala, October 14, 2010