Company
FranceSERIPHARM, Le Mans, France – FDA Inspections
Inspection records and compliance data for SERIPHARM in Le Mans. 5 FDA inspections on record, last inspected March 12, 2021.
Company Profile
This profile covers SERIPHARM based in Le Mans, France.
FDA Inspection History
- FDA inspections
- 5
- OAI
- 0
- VAI
- 3
- NAI
- 2
- Form 483s
- 0
- Warning letters
- 0
First inspected January 29, 2010. Last inspected March 12, 2021.
FDA inspections (5)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| March 12, 2021 | NAI | Human Drugs · Drug Quality Assurance | 1273405 |
| March 15, 2018 | VAI | Human Drugs · Drug Quality Assurance | 1068502 |
| May 6, 2016 | NAI | Human Drugs · Drug Quality Assurance | 972558 |
| June 6, 2013 | VAI | Human Drugs · Drug Quality Assurance | 836916 |
| January 29, 2010 | VAI | Human Drugs · Drug Quality Assurance | 646917 |
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
SERIPHARM
FEI Number
3002808119
Address
Technopole Universite, 1 rue Democrite, Le Mans, France
Country
France
ID: b5349d82-bf7e-4e82-b09e-2c134d55df09