FDA Inspection 1163524 — RMA Long Island IVF

RMA Long Island IVF — FEI 3007067646

The FDA completed an inspection of RMA Long Island IVF on Mar 1, 2022 in Melville, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 1, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Melville, NY (United States)

Citations

IDCFRDescription
1222921 CFR 1271.50(a)Determination based on screening and testing