# PMT Corporation - Inspection Records

Source: https://www.keypedia.com/companies/pmt-corporation/cc2a9d50-0fa4-4e0c-b246-dc5793a64f06

> Inspection records and compliance data for PMT Corporation in Chanhassen, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: PMT Corporation
- FEI Number: 2182979
- City: Chanhassen
- State: Minnesota
- Country Name: United States
- Address Line 1: 1500 Park Rd
- Zip Code: 55317

## Related Documents

- [483 - PMT Corporation - 2024-02-15](https://www.keypedia.com/records/483/pmt-corporation/b1334084-cd6c-4cd1-ba03-7f016c143491) — source: FDA, date: February 15, 2024
- [FDA Inspection 1229837 - PMT Corporation - 2024-02-15](https://www.keypedia.com/records/fda_inspections/pmt-corporation/cd9f7b5e-f402-4282-9bb9-446945203412) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 15, 2024
- [FDA Inspection 1008552 - PMT Corporation - 2017-03-23](https://www.keypedia.com/records/fda_inspections/pmt-corporation/c3cb91eb-bb71-4c75-93cf-b7b41fe7a3cc) — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2017
- [FDA Inspection 831607 - PMT Corporation - 2013-06-06](https://www.keypedia.com/records/fda_inspections/pmt-corporation/ace1b1a7-a517-45f3-ad10-6fa669bfc2ca) — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2013
- [FDA Inspection 673753 - PMT Corporation - 2010-07-16](https://www.keypedia.com/records/fda_inspections/pmt-corporation/5e0f5436-f4fe-4b37-914b-7c106838e6d4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 16, 2010
- [FDA Inspection 600960 - PMT Corporation - 2009-08-04](https://www.keypedia.com/records/fda_inspections/pmt-corporation/363cf8c4-c5b2-4a1f-8c05-18382ec996ce) — classification: Official Action Indicated (OAI), source: FDA, date: August 4, 2009
- [FDA Inspection 600960 - PMT Corporation - 2009-08-04](https://www.keypedia.com/records/fda_inspections/pmt-corporation/d4c2a18a-b0bf-4bf1-8347-5892d45289f8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 4, 2009

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