FDA Inspection 940147 — Manhattan Regenerative Medicine Medical Group

Manhattan Regenerative Medicine Medical Group — FEI 3011770053

The FDA completed an inspection of Manhattan Regenerative Medicine Medical Group on September 19, 2015 in New York, NY. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 9 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 19, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
New York, NY (United States)

Citations

IDCFRDescription
111221 CFR 211.25(a)Training--operations, GMPs, written procedures
117721 CFR 211.63Equipment Design, Size and Location
145121 CFR 211.113(b)Procedures for sterile drug products
183321 CFR 211.84(d)(1)Identity Testing of Each Component
188521 CFR 211.165(b)Microbiological testing
360321 CFR 211.160(b)Scientifically sound laboratory controls
436921 CFR 211.188(b)(11)Identification of persons involved, each significant step
441821 CFR 211.42(b)Adequate space lacking to prevent mix-ups and contamination
900121 CFR 211.22(a)Lack of quality control unit