The low-lying electron states of ozone are studied using anion photoelectron spectroscopy of O-3. The spectra show photodetachment transitions from 0(3)(-) to the ($) over tilde X(1)A(1) ground state and to the five lowest lying electronic states of the ozone molecule, namely the (3)A(2), B-3(2), (1)A(2), B-3(1), and B-1(1) states. The geometry of the ozonide anion determined from a Franck-Condon analysis of the O(3)X(1)A(1) ground state spectrum agrees reasonably well with previous work. The excited state spectra are dominated by bending vibrational progressions which, for some States, extend well above the dissociation asymptote without noticeable lifetime broadening effects. Preliminary assignments are based upon photoelectron angular distributions and comparison with ab initio calculations. None of the excited states observed lies below the ground state dissociation limit of O-3 as suggested by previous experimental and theoretical results.