The resonance-enhanced multiphoton ionization (REMPI) spectrum of formaldehyde, two photon resonant in the region of the (1)A(2)(3p(x)), (1)A(1)(3p(y)), and B-1(2)(3p(z)) states, is reported. The (1)A(2)(3p(x)) state spectrum is dominated by the nu (')(3) (CH2 scissors), nu (4)' (CH2 out-of-plane bending), nu (')(5) (CH2 asymmetric stretching), and nu (')(6) (CH2 rock) modes, with weaker bands observed for excitation of the nu (2)' (CO stretching) mode. Vibrational analysis of the spectrum provides many new frequencies for the (1)A(2)(3p(x)) state, not resolved or accessible in single photon spectroscopic measurements. Photoelectron spectroscopy is used to probe the nature of the vibronic levels associated with the (1)A(2)(3p(x)) intermediate state, to measure vibrational frequencies of the resulting cations, and to identify useful routes for preparing vibrational state-selected H2CO+. It is found that H2CO[(1)A(2)(3p(x))] is a well-behaved Rydberg state, generating cations in the same vibrational level that was populated in the intermediate. Cations with mode-selective excitation of up to 0.62 eV can be produced. Ab initio calculations are used to help assign the cation vibrations. In contrast to the well-behaved (1)A(2)(3p(x)) state, the (1)A(1)(3p(y)) and B-1(2)(3p(z)) states are strongly mixed with each other and with valence states.