# FDA Inspection 1056342 - Polymicro Technologies, Molex Llc - April 27, 2018

Source: https://www.keypedia.com/records/fda_inspections/polymicro-technologies-molex-llc/f5a04f96-cea8-4b71-84a4-d6666547cb63
Source feed: FDA_Inspections

> FDA Inspection 1056342 for Polymicro Technologies, Molex Llc on April 27, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1056342
- Company Name: Polymicro Technologies, Molex Llc
- Inspection Date: 2018-04-27
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1056342 - 2018-04-27](https://www.keypedia.com/records/fda_inspections/polymicro-technologies-molex-llc/5c830576-1ee4-4baa-b1bb-4d4e54a0600a)
- [FDA Inspection 1056342 - 2018-04-27](https://www.keypedia.com/records/fda_inspections/polymicro-technologies-molex-llc/8c625cec-7522-4441-b4ea-fef868b6a17d)

Company: https://www.keypedia.com/companies/polymicro-technologies-molex-llc/40178caf-cd5e-4ea0-8cd3-5fde17d3f0af

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7