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Pre Inspection Plan

Company Name :

Notes from site master files


- SMF Document Number:

- Production Lines:

- QC. Lab:( contract or not)

- List Of Product:

Notes from previous inspection report (Company compliance history) –If Applicable-

Quality Defects cases/Recalls

Medicinal product submitted to JFDA for registration

JFDA Page 1 of 2 FR03/FAC/01


Pre Inspection Plan

Note

Inspectors Name Signature


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JFDA Page 2 of 2 FR03/FAC/01

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