# FDA Inspection 896199 - KEDPLASMA LLC - September 18, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/9e6a2753-8796-4851-92b0-c4ca52f664ec
Source feed: FDA_Inspections

> FDA Inspection 896199 for KEDPLASMA LLC on September 18, 2014. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 896199
- Company Name: KEDPLASMA LLC
- Inspection Date: 2014-09-18
- 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 1053816 - 2018-05-03](https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/6ffa85db-ab76-4796-9fcb-0a14a0907167)
- [FDA Inspection 778966 - 2012-04-27](https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/6e9c8c27-698f-40fb-8a75-d3bb20588b39)

Company: https://www.globalkeysolutions.net/companies/kedplasma-llc/f369f19e-f8f5-4f66-ba28-cf5a53b0c70d

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