What's New Unreplied Topics Membership About Us Contact Us Privacy Policy
[Ad]

Corrective action when records are not completed?

Started by , Jul 31 2014 01:11 PM
6 Replies

Dear friends,

 

for example the chemist do not documented records from 18.7.2014, how to  write a corrective action

any one please help me , how to satisfied the auditor?

Share this Topic
Topics you might be interested in
Corrective Actions for a FCS tested positive on Listeria spp Verification Report Missed - is this a non-conformity with a corrective action? Corrective Action Resolution with NSF Audit Corrective action for Allergen recall How long does it take the Certification Body to approve a submitted Corrective Action Report?
[Ad]

Dear friends,

 

for example the chemist do not documented records from 18.7.2014, how to  write a corrective action

any one please help me , how to satisfied the auditor?

 

Dear prembibo,

 

Apologies but the above is unintelligible.

 

Please rewrite with relevant context.

 

Rgds / Charles.C

 

PS - and maybe post in a more relevant forum ?

1 Thank
What I think I understood from your text is that someone failed to do their required checks or tests on July 18th, 2014. Is the case, I would suggest giving that person a documented warning that they did not perform their job to expectations. Give them a place to reply on this documentation and you should keep a copy for the auditor if that error should get noticed.

It is the documention that you addressed the erros that the auditor will want to see.

Hope that helps!
1 Thank

I would also add that the person is not to work unsupervised until they have undergone retraining

 

Caz

3 Thanks

If it's some sort of HACCP or Pre-requisite record be sure to go back and prove that all your product being produced for that date has undergone review and all aspects of food safety are found to be acceptable

3 Thanks

If one of my employees did not document the records then there is no way you can prove the all of your critical steps were met. I would discard the products and have a disciplinary meeting with the employee that was responsible to document the information. Make sure you document the discarding of the product i.e. how much (the USDA makes us use total weight of product), when you did it, and where it went. Also, document the meeting with your employees by having them sign a sheet (a warning letter). You could also hold a retraining class for all employees involved in the process and document that.

1 Thank

Dear prembibo,

 

The following will act as CA,

i) Write an internal memo reminding the chemist his duties and responsibility.

ii) Include the responsible to check the records periodically e.g the supervisor

iii) retrain the chemist on the control of documents Clause 4.2.3 and its importance to the operations.

3 Thanks

Similar Discussion Topics
Corrective Actions for a FCS tested positive on Listeria spp Verification Report Missed - is this a non-conformity with a corrective action? Corrective Action Resolution with NSF Audit Corrective action for Allergen recall How long does it take the Certification Body to approve a submitted Corrective Action Report? Corrective Actions: When to Document Non-Conformances and Deviations Listeria Innocua corrective actions Corrective Actions - Presumptive Positive Listeria Spp. in Processing Corrective Action Request Template Guidelines for Corrective and Preventive Actions for Carcass Core Temperature CCP in Chicken Processing