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Equipment Malfunction and Corrective Action Record: Storage Equipment and Plasma Thawed Effective Date: 31MAR2011 Approved by: Document # F160QCFORM15 Version # 01 Source Documents: Manitoba Transfusion
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How to fill out f160-qcform-15 equipment malfunction and:

01
Start by entering your personal information such as your name, address, and contact details.
02
Identify the specific equipment that experienced the malfunction and provide details such as the equipment name, model number, and serial number.
03
Describe the malfunction in detail, including any error messages or unusual behavior exhibited by the equipment.
04
Indicate the date and time when the malfunction occurred. If the malfunction is ongoing, mention the duration.
05
Specify whether any troubleshooting or repairs have been attempted and provide details if applicable.
06
If there were any witnesses to the malfunction, include their names and contact information.
07
Lastly, sign and date the form to acknowledge the accuracy and truthfulness of the information provided.

Who needs f160-qcform-15 equipment malfunction and:

01
Individuals who have experienced equipment malfunctions and wish to report them.
02
Technicians or support staff responsible for addressing equipment malfunctions.
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Organizations or companies that require documentation and records of equipment malfunctions for regulatory or compliance purposes.
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