I has experience blunting with klenow after PCR. After PCR reaction remove dNTP and primers using a purification PCR column (as quiagen). Then incubate the DNA with klenow for 5 min at 37 C, add dNTP and incubate for additional 15 min. Stop the reaction and use for ligation
I guest the protocol for your polymerase should be the same using the appropriate Temp