Company
United StatesCorflex, Inc., Manchester, NH – FDA Inspections
Inspection records and compliance data for Corflex, Inc. in Manchester, New Hampshire. 1 FDA inspection on record, 1 Form 483, last inspected January 04, 2017.
Company Profile
This profile covers Corflex, Inc. based in Manchester, New Hampshire, United States.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 1
- NAI
- 0
- Form 483s
- 1
- Warning letters
- 0
Inspected January 4, 2017.
Most cited issue areas
- Complaints1 inspection
- Lack of or inadequate complaint procedures1 inspection
- Lack of Written MDR Procedures1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| January 4, 2017 | VAI | Medical Devices & Rad Health · Compliance: Devices | 997339 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
Corflex, Inc.
FEI Number
1218997
Address
669 E Industrial Park Dr, Manchester, New Hampshire 03109, United States
Country
United States
ID: 8666c05f-6c13-4eed-8d63-639e7385ef3e