Industrial Woodworking Corp.
9380 Pentatech Dr., Zeeland, MI, US
Registered product codes
1 product codes
Recent MDR events
0 on file
No MDR events on file for this firm name.
Recalls
0 on file
No recalls on file for this firm name.
Compliance history
Matched by FEI 3003904216.
FDA inspections
2 on file
- Voluntary Action Indicated (VAI)Mar 12, 2025
Compliance: Devices · Citations posted
- No Action Indicated (NAI)Mar 12, 2025
Postmarket Assurance: Devices · Citations posted
Inspection citations
8 on file
Top cited requirements
Compare to industry ↗21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
121 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
121 CFR 820.75(a)Lack of or inadequate process validation
121 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
121 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
121 CFR 820.184DHR content
1
- 21 CFR 820.70(a)Mar 12, 2025
Process control procedures, Lack of or inadequate procedures
- 21 CFR 820.70(g)(1)Mar 12, 2025
Maintenance schedule, Lack of or inadequate schedule
- 21 CFR 820.75(a)Mar 12, 2025
Lack of or inadequate process validation
- 21 CFR 820.75(b)Mar 12, 2025
Lack/Inad procedure-Monitoring/Control of Validated Proces
- 21 CFR 820.90(a)Mar 12, 2025
Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.184Mar 12, 2025
DHR content
- 21 CFR 820.198(a)Mar 12, 2025
Lack of or inadequate complaint procedures
- 21 CFR 820.250(b)Mar 12, 2025
Sampling plans
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.