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 3009424796.
Observations7
Issue DateJuly 22, 2021
StatusNo Warning Letter
Related Inspections6
Establishment Details
Firm
Kelyniam Global, Inc.
Location
Collinsville, Connecticut, United States
FEI Number
3009424796
Product Type
Devices
Issue Date
July 22, 2021
Country
United States
Inspection History, 2013 to 2024
VAI5
OAI1
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
Talk to a Specialist