Company
United StatesSynedgen Inc., Claremont, CA – FDA Inspections
Inspection records and compliance data for Synedgen Inc. in Claremont, California. 1 FDA inspection on record, 1 Form 483, last inspected July 26, 2019.
Company Profile
This profile covers Synedgen Inc. based in Claremont, California, United States.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 0
- NAI
- 1
- Form 483s
- 1
- Warning letters
- 0
Inspected July 26, 2019.
Most cited issue areas
- Management review - Lack of or inadequate procedures1 inspection
- Quality Audit/Reaudit - conducted1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| July 26, 2019 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1097763 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Synedgen Inc.
FEI Number
3008663070
Address
1420 N Claremont Blvd Ste 105d, Claremont, California 91711, United States
Country
United States
ID: a1d04c3b-ea1c-4d03-a484-5cd727c38e34