Company
United StatesMaxiFlex, LLC, New Orleans, LA – FDA Inspections
Inspection records and compliance data for MaxiFlex, LLC in New Orleans, Louisiana. 2 FDA inspections on record, 1 Form 483, last inspected December 20, 2018.
Company Profile
This profile covers MaxiFlex, LLC based in New Orleans, Louisiana, United States.
FDA Inspection History
- FDA inspections
- 2
- OAI
- 0
- VAI
- 0
- NAI
- 2
- Form 483s
- 1
- Warning letters
- 0
First inspected May 11, 2011. Last inspected December 20, 2018.
Most cited issue areas
- Complaints1 inspection
- Lack of or inadequate procedures1 inspection
FDA inspections (2)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| December 20, 2018 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1075109 |
| May 11, 2011 | NAI | Medical Devices & Rad Health · Compliance: Devices | 734724 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
MaxiFlex, LLC
FEI Number
3006812215
Address
512 Verret St, New Orleans, Louisiana 70114, United States
Country
United States
ID: 77a1952f-edeb-44bd-a2bb-b3773680959b