# Kedplasma LLC - Inspection Records

Source: https://www.keypedia.com/companies/kedplasma-llc/4bb706c9-c8b4-43d0-99e7-6c0400611d45

> Inspection records and compliance data for Kedplasma LLC in Temple Terrace, Florida. Access full analysis and detailed observations.

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## Details

- Name: Kedplasma LLC
- FEI Number: 3004158206
- City: Temple Terrace
- State: Florida
- Country Name: United States
- Address Line 1: 5252 E Fowler Ave
- Zip Code: 33617

## Related Documents

- [FDA Inspection 1295862 - Kedplasma LLC - 2025-12-10](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/36398974-7753-4536-b4d9-b7783441f5aa) — source: FDA, date: December 10, 2025
- [FDA Inspection 1295862 - Kedplasma LLC - 2025-12-10](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/e83a3f3b-d6a3-41e1-96c2-c961daf8fd0c) — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2025
- [FDA Inspection 1032352 - Kedplasma LLC - 2017-10-09](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/17395f04-f69a-4b9f-a15f-f8e8166201b9) — classification: No Action Indicated (NAI), source: FDA, date: October 9, 2017
- [FDA Inspection 944212 - Kedplasma LLC - 2015-09-30](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/5902d68d-4276-4b9b-a294-e5fbcedd62cf) — classification: No Action Indicated (NAI), source: FDA, date: September 30, 2015
- [FDA Inspection 830577 - Kedplasma LLC - 2013-05-07](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/191d43b9-8b21-4854-9483-ccbd7070a512) — classification: No Action Indicated (NAI), source: FDA, date: May 7, 2013
- [FDA Inspection 718683 - Kedplasma LLC - 2011-04-08](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/2a44641c-54ca-4f41-bd79-4a1363d37cc9) — classification: No Action Indicated (NAI), source: FDA, date: April 8, 2011
- [FDA Inspection 555184 - Kedplasma LLC - 2009-01-08](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/ad9445c6-3bd9-4bee-aa37-d8ea5d4767b9) — classification: No Action Indicated (NAI), source: FDA, date: January 8, 2009

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