Pro-Tech Design & Manufacturing, Inc.
FDA Regulatory Profile
Pro-Tech Design & Manufacturing, Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.
- Latest inspection
- Jun 27, 2025 · VAI
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 6 | Nov 11, 2026 | Newest record Nov 5, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| Jun 27, 2025 | Santa Fe Springs, CA | Devices | Voluntary Action Indicated (VAI) | 3003574398 |
| Jun 27, 2025 | Santa Fe Springs, CA | Devices | No Action Indicated (NAI) | 3013023969 |
| Mar 16, 2022 | Santa Fe Springs, CA | Devices | No Action Indicated (NAI) | 3003574398 |
| Mar 16, 2018 | Santa Fe Springs, CA | Devices | No Action Indicated (NAI) | 3003574398 |
| Jul 27, 2016 | Santa Fe Springs, CA | Devices | No Action Indicated (NAI) | 3003574398 |
| Jun 12, 2014 | Santa Fe Springs, CA | Devices | Voluntary Action Indicated (VAI) | 3003574398 |
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.