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 1000125324.
Observations2
Issue DateJanuary 30, 2020
StatusNo Warning Letter
Related Inspections10
Establishment Details
Firm
PureTek Corporation
Location
San Fernando, California, United States
FEI Number
1000125324
Product Type
Drugs
Issue Date
January 30, 2020
Country
United States
Inspection History, 2010 to 2025
NAI2
VAI8
NAI means No Action Indicated. VAI means Voluntary Action Indicated.