Facility Inspection Procedure
SKU:
SOP 6-006
$149.00
$149.00
per item
The ISO 13485 Facility Inspection Procedure defines the process and responsibilities for handling facility inspections conducted by FDA, Notified Bodies, Government Agencies and other third-party inspections.
- ISO 13485 Compliant
- FDA QSR Compliant
- MS Word Format
- Digital Content - Instant Download
Facility Inspection ProcedureThe Facility Inspection Procedure defines the process and responsibilities for handling facility inspections conducted by FDA, Notified Bodies, Government Agencies and other third-party inspections.
Facility Inspection Procedure - OverviewThe Facility Inspection Procedure identifies assigned inspection personnel and alternates, assigns responsibilities for multiple types of inspections. The Facility Inspection Procedure provides instruction on inspection restrictions and the proper internal handling of facility inspections and inspectors. The procedure also includes instruction on exit interviews, and timelines for required post inspection activities.
Facility Inspection Procedure - ComplianceThe Facility Inspection Procedure is ISO 13485:2016 and FDA 21 CFR Part 820 compliant.
For more information about our ISO 13485 Facility Inspection Procedure contact us at info@aplyon.com
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