Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3013501947.
Observations2
Issue DateApril 17, 2019
StatusNo Warning Letter
Establishment TypeProducer of Non Sterile Drug Products
Related Inspections0
Establishment Details
Firm
Kohana Pharmacy and Center for Regenerative Medicine Inc.
Location
California, United States
FEI Number
3013501947
Establishment Type
Producer of Non Sterile Drug Products
Product Type
Drugs
Issue Date
April 17, 2019
Country
United States
Inspection History
We hold no FDA inspection matched to this establishment.
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