# FDA Inspection 1205319 - TelaGen, LLC - January 30, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/telagen-llc/de3a6a5f-b668-47a0-a439-2b087a4b139a
Source feed: FDA_Inspections

> FDA Inspection 1205319 for TelaGen, LLC on January 30, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1205319
- Company Name: TelaGen, LLC
- Inspection Date: 2023-01-30
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1205319 - 2023-01-30](https://www.globalkeysolutions.net/records/fda_inspections/telagen-llc/10c20cf8-e140-439c-b716-0e3863e5eb06)
- [FDA Inspection 1205319 - 2023-01-30](https://www.globalkeysolutions.net/records/fda_inspections/telagen-llc/c65b720b-bd70-4365-8228-6b5925d46205)
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- [FDA Inspection 1028498 - 2017-06-06](https://www.globalkeysolutions.net/records/fda_inspections/telagen-llc/690db77b-e6e5-4d71-820a-b4f6bf826385)

Company: https://www.globalkeysolutions.net/companies/telagen-llc/1874802a-339a-45c8-857f-e6dae8dc567e

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