Company
United StatesFlexDex Inc., Brighton, MI – FDA Inspections
Inspection records and compliance data for FlexDex Inc. in Brighton, Michigan. 1 FDA inspection on record, 1 Form 483, last inspected June 22, 2017.
Company Profile
This profile covers FlexDex Inc. based in Brighton, Michigan, United States.
FDA Inspection History
- FDA inspections
- 1
- OAI
- 0
- VAI
- 1
- NAI
- 0
- Form 483s
- 1
- Warning letters
- 0
Inspected June 22, 2017.
Most cited issue areas
- Acceptable supplier records, inadequate records1 inspection
FDA inspections (1)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| June 22, 2017 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1015191 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
FlexDex Inc.
FEI Number
3012046682
Address
10421 Citation Dr Ste 900, Brighton, Michigan 48116, United States
Country
United States
ID: a2369927-5ba8-4328-9a0f-d52f3e6d83a6