# FDA Inspection 1092892 - telaGen, LLC - April 04, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/telagen-llc/1c9d2fd9-2e2d-4d4d-9b4b-76014cd65f4d
Source feed: FDA_Inspections

> FDA Inspection 1092892 for telaGen, LLC on April 04, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1092892
- Company Name: telaGen, LLC
- Inspection Date: 2019-04-04
- Classification: No Action Indicated (NAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1092892 - 2019-04-04](https://www.globalkeysolutions.net/records/fda_inspections/telagen-llc/3cc6d6f5-640a-4d4d-995f-4db6c772bdf5)

Company: https://www.globalkeysolutions.net/companies/telagen-llc/230da4f4-f06a-4ac7-8399-3538aa38e68d

Office: https://www.globalkeysolutions.net/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d