Company
United StatesDynaFlex, Lake Saint Louis, MO – FDA Inspections
Inspection records and compliance data for DynaFlex in Lake Saint Louis, Missouri. 4 FDA inspections on record, 4 Form 483s, last inspected March 06, 2026.
Company Profile
This profile covers DynaFlex based in Lake Saint Louis, Missouri, United States.
FDA Inspection History
- FDA inspections
- 4
- OAI
- 0
- VAI
- 2
- NAI
- 1
- Unclassified
- 1
- Form 483s
- 4
- Warning letters
- 0
First inspected April 18, 2018. Last inspected March 6, 2026.
Most cited issue areas
- Acceptable supplier records, inadequate records1 inspection
- Calibration, Inspection, etc. Procedures Lack of or Inadequ1 inspection
- Equipment calibration or verification not performed1 inspection
FDA inspections (4)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| March 6, 2026 | Not classified | Medical Devices & Rad Health · Compliance: Medical Devices | 1305824 |
| September 25, 2023 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1218587 |
| September 5, 2019 | VAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1102731 |
| April 18, 2018 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1048804 |
FDA documents
People (1)
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
DynaFlex
FEI Number
1937100
Address
8050 Hawk Ridge Trl, Lake Saint Louis, Missouri 63367, United States
Country
United States
ID: a805d418-c220-4dcf-8f82-08ee4c075100