Company
ItalyNeotron S.p.A, Modena, Italy – FDA Inspections
Inspection records and compliance data for Neotron S.p.A in Modena. 3 FDA inspections on record, 1 Form 483, last inspected February 23, 2023.
Company Profile
This profile covers Neotron S.p.A based in Modena, Italy.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 2
- NAI
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected July 7, 2017. Last inspected February 23, 2023.
Most cited issue areas
- Calibration/Inspection/Checking not done1 inspection
- Extent of discrepancy, failure investigations1 inspection
- Quality control unit review of records1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| February 23, 2023 | VAI | Human Drugs · Drug Quality Assurance | 1276129 |
| September 6, 2019 | VAI | Human Drugs · Drug Quality Assurance | 1101319 |
| July 7, 2017 | NAI | Human Drugs · Drug Quality Assurance | 1022356 |
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
Neotron S.p.A
FEI Number
3011749590
Address
Stradello Aggazzotti 104, Modena, Italy
Country
Italy
ID: 7e4ca124-0b66-41ba-8a9e-a1aecba08075