Information

  • Audit Title

  • Document No.

  • Client / Site

  • Conducted on

  • Prepared by

  • Location
  • Personnel

Product Analysis

  • Has finished product testing been completed to ensure compliance with specifications?

  • Are all products sampled to determine quality standards?

  • Are shelf life samples drawn per batch where applicable and stored at optimum conditions for the duration of the shelf-life of the product?

  • Are suitable procedures in place governing sampling methods, samples and testing?

  • Have all staff tasked with sampling, qc checks, ect. received documented training against the relevant procedures?

  • Are documented procedures in place to cover documenting and reporting routine as well as out-of-spec results?

Labeling and Product Coding

  • Are all products conforming to finished product specifications?

  • Is a labeling and coding procedure in place?

  • Are all personnel carrying out labeling and coding checks trained against the procedure?

Volume, Weight and Count Management

  • Is a documented procedure available for the control of volume, weight and count for products manufactured?

  • Are weight, volume and tare verification checks completed daily on every production run?

  • Do all scales and equipment used for finished product weight verification checks undergo calibration verification at least once daily?

  • Are checks being done to verify the count/number of products in a box?

  • Are product drained weights verified on a pre-determined frequency to confirm accuracy?

  • Have all personnel involved in the management of product weight, volume and count been trained?

Allergen Management

  • Is there an allergen risk matrix available for all products and is it up to date?

  • Has an allergen risk assessment been conducted?

  • Is there a list of allergens available?

  • No risk of allergens in production area?

  • Any outside risk for allergen contamination controlled?

General Quality Control

  • Are all products tested and released by lab prior to dispatch?

  • Is lab equipment calibration verified on a daily basis?

  • Are all applicable quality analysis and control documentation on file and up to date?

  • Are all products tested in the last month conforming to specifications?

  • Are all non-conformance issues appropriately logged and actions taken appropriate?

  • Are all quality documentation, records and inspection sheets appropriately signed off and filed?

  • Are all orders checked on loading and dispatch?

  • Is organic and fair trade product integrity in tact?

  • Are trained quality technologists readily available on site?

  • Is an organogram in place showing technical succession?

  • Is quality control effectively managed?

  • No major non-conformances pertaining to quality observed during inspection?

The templates available in our Public Library have been created by our customers and employees to help get you started using SafetyCulture's solutions. The templates are intended to be used as hypothetical examples only and should not be used as a substitute for professional advice. You should seek your own professional advice to determine if the use of a template is permissible in your workplace or jurisdiction. You should independently determine whether the template is suitable for your circumstances.