Company
United StatesSynovo Production, Fullerton, CA – FDA Inspections
Inspection records and compliance data for Synovo Production in Fullerton, California. 3 FDA inspections on record (2 OAI), 1 Form 483, last inspected June 12, 2025.
Company Profile
This profile covers Synovo Production based in Fullerton, California, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 2
- VAI
- 1
- NAI
- 0
- Form 483s
- 1
- Warning letters
- 0
First inspected October 26, 2022. Last inspected June 12, 2025.
Most cited issue areas
- Training records2 inspections
- Design changes - Lack of or Inadequate Procedures1 inspection
- Design history file1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| June 12, 2025 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1276066 |
| October 2, 2023 | OAI | Medical Devices & Rad Health · Compliance: Devices | 1219420 |
| October 26, 2022 | OAI | Medical Devices & Rad Health · Compliance: Devices | 1182099 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Synovo Production
FEI Number
2280596
Address
1501 N Harbor Blvd Ste 209, Fullerton, California 92835, United States
Country
United States
ID: e55218cc-2f72-4106-8604-f7d9a0bc58d6