# FDA 483 - Theo Manufacturing BV - May 22, 2019

Source: https://www.globalkeysolutions.net/records/483/theo-manufacturing-bv/5bf20eaa-9a12-4318-8a48-bc8420285ba8

> FDA 483 for Theo Manufacturing BV on May 22, 2019. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Theo Manufacturing BV
- Inspection Date: 2019-05-22
- Product Type: device
- Office Name: Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)

## Related Officers

- [Dedicated Device Cadre](https://www.globalkeysolutions.net/people/dedicated-device-cadre/693932db-dd86-453f-9b51-a63444b07281)
- [investigator](https://www.globalkeysolutions.net/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.globalkeysolutions.net/companies/theo-manufacturing-bv/6d060981-3de3-47d9-be41-ff5afa47cb0c

Office: https://www.globalkeysolutions.net/offices/division-of-clinical-evidence-and-analysis-1-clinical-policy-and-quality/5f95da17-30bb-423f-b892-5ea041823fbd