FDA Inspection 1028527 — Kaiser Permanente Of The Mid-Atlantic States IRB #7

Kaiser Permanente Of The Mid-Atlantic States IRB #7 — FEI 3013826200

The FDA completed an inspection of Kaiser Permanente Of The Mid-Atlantic States IRB #7 on Oct 10, 2017 in Rockville, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.