Source: FDA record for this establishment. FDA publishes inspections or enforcement actions for this establishment, listed further down this page, but we have not matched this particular Form 483 to a document or an inspection date FDA has released. It stays out of the default view for that reason. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3007137482.
Observations4
Issue DateFebruary 03, 2010
Status1 Related Warning Letter
Related Inspections10
Establishment Details
Firm
Diasol, Inc
Location
Phoenix, Arizona, United States
FEI Number
3007137482
Product Type
Devices
Issue Date
February 03, 2010
Country
United States
Inspection History, 2010 to 2025
NAI3
VAI3
OAI4
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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