# FDA Inspection 1208520 - Techlem Medical Corporation - June 22, 2023

Source: https://www.keypedia.com/records/fda_inspections/techlem-medical-corporation/3c240164-b1a1-422d-8c67-8f5b655cd352
Source feed: FDA_Inspections

> FDA Inspection 1208520 for Techlem Medical Corporation on June 22, 2023. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1208520
- Company Name: Techlem Medical Corporation
- Inspection Date: 2023-06-22
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1208520 - 2023-06-22](https://www.keypedia.com/records/fda_inspections/techlem-medical-corporation/e933f19f-fd37-4f82-9016-b66fefe56c99)
- [FDA Inspection 821084 - 2013-02-28](https://www.keypedia.com/records/fda_inspections/techlem-medical-corporation/c9238efa-fe0b-44db-b057-35ecd64b8d74)
- [FDA Inspection 821084 - 2013-02-28](https://www.keypedia.com/records/fda_inspections/techlem-medical-corporation/4cf1c5de-fbd4-4828-9ce0-7fd72326e874)

Company: https://www.keypedia.com/companies/techlem-medical-corporation/7f5d026a-9683-4afa-9d48-0a4539c77bb4

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