Greetings Compliance Experts.

 

Something disturbing came across my desk today I thought I would get your
opinion on it.

 

On a CE marked peripheral we buy/sell as part of our laboratory equipment
system, failed several immunity tests when we tested it as part of our system.
 When we notified the peripheral's manufacturer of the problem (yes, I'm being
purposely vague) they said the failures were ok and sent us a "Certificate of
Compliance" by a very very well know compliance lab with the following
statement:

 

Snip

 

EMC Immunity:

EN 61326-1:1997/A1:1998/A2:2001 EMC requirements for Electrical equipment for
measurement, control, and laboratory use.

- General Use for the following test with deviation of performance criteria to
Criteria "C" instead of "B".

EN 61000-4-2

EN 61000-4-3

EN 61000-4-4

 

Unsnip

 

 

The peripheral manufacture said the EMC test lab told them they can put the CE
marking on their product as long as they included the above deviation
statement in their documentation and DOC.  

 

Is this true or was there some kind of miscommunication between the test lab
and the peripheral manufacturer?  

 

With this line of thinking, our test lab will not have to fail anything in the
future; just pass it with a deviation in the requirements. (just kidding).

 

Thanks to all for your opinion.

 

The Other Brian

 

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