FDA Inspection 659029 — Mollen, Martin D., MD

Mollen, Martin D., MD — FEI 3003586092

The FDA completed an inspection of Mollen, Martin D., MD on Apr 7, 2010 in Phoenix, AZ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 4 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 7, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Phoenix, AZ (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
752021 CFR 312.64(b)Safety reports
753021 CFR 312.62(b)Case history records- inadequate or inadequate
755221 CFR 312.66Changes in research
756021 CFR 312.60FD-1572, protocol compliance