Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3006446551.
ObservationsNot available
Issue DateFebruary 09, 2023
StatusNo Warning Letter
Related Inspections6
Establishment Details
Firm
Ambiopharm, Inc.
Location
Beech Island, South Carolina
FEI Number
3006446551
Product Type
Drugs
Issue Date
February 09, 2023
Country
United States
Inspection History, 2008 to 2023
NAI2
VAI4
NAI means No Action Indicated. VAI means Voluntary Action Indicated.