FDA Inspection 877715 — Robert J. Weiss, M.D.

Robert J. Weiss, M.D. — FEI 1000120371

The FDA completed an inspection of Robert J. Weiss, M.D. on May 12, 2014 in Auburn, ME. 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). 3 citations were issued during this inspection. Product area: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 12, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Auburn, ME (United States)

Additional details

Clinical Investigator (CI)

Citations

IDCFRDescription
751721 CFR 312.66Initial and continuing review
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance

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