In this work a new strategy for the automation of the standard addition method by FIA with voltammetric detection is described, based on the concept of multi‐site detection. In the system developed, a single voltammetric detector with mobility in the FIA manifold, carried out sequential measurement of the sample plug before and after addition of the standard solution. The construction and evaluation of the voltammetric detector of tubular configuration and internal diameter similar to the tubing of the FIA manifold, whose incorporation in the system allowed the measurement process to be carried out without change of the hydrodynamic characteristics of the sample plug, is also mentioned. To evaluate the usefulness of the proposed multi‐site voltammetric detection system, this was used in the amperometric determination of ascorbic acid in fruit juices where the standard addition method is frequently required to overcome the matrix effect. The results obtained with the FIA system were compared with those from the reference procedure proposed by AOAC. No statistical difference between methods was found at the 95% confidence level. The relative deviations between both methods were always less than or equal to 3.8%. The sampling rate was about 55 samples per hour (110 measurements).