# Kindeva Drug Delivery LP - Inspection Records

Source: https://www.keypedia.com/companies/kindeva-drug-delivery-lp/f2c804ad-6a24-440f-bc37-8b00b76e1de3

> Inspection records and compliance data for Kindeva Drug Delivery LP in Northridge, California. Access full analysis and detailed observations.

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## Details

- Name: Kindeva Drug Delivery LP
- FEI Number: 2010441
- City: Northridge
- State: California
- Country Name: United States
- Address Line 1: 19901 Nordhoff St
- Zip Code: 91324
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK

## Related Documents

- [483 - Kindeva Drug Delivery LP - 2025-11-13](https://www.keypedia.com/records/483/kindeva-drug-delivery-lp/772d01d4-412d-4ee3-b9bb-0bc89003aeeb) — source: FDA, date: November 13, 2025
- [FDA Inspection 1286864 - Kindeva Drug Delivery LP - 2025-11-13](https://www.keypedia.com/records/fda_inspections/kindeva-drug-delivery-lp/b37641bf-e88e-489b-abd5-0192feee2887) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 13, 2025
- [483 - Kindeva Drug Delivery LP - 2024-04-03](https://www.keypedia.com/records/483/kindeva-drug-delivery-lp/0e22ea50-be1c-45d3-b2d5-6a2c7eb97832) — source: FDA, date: April 3, 2024
- [FDA Inspection 1151074 - Kindeva Drug Delivery LP - 2021-07-28](https://www.keypedia.com/records/fda_inspections/kindeva-drug-delivery-lp/051a73f4-4ead-4626-b3ed-832dc0f0b751) — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2021
- [FDA Inspection 1082205 - Kindeva Drug Delivery LP - 2019-01-25](https://www.keypedia.com/records/fda_inspections/kindeva-drug-delivery-lp/6ea1bb22-ffb8-4f18-967a-789df7b29aa9) — classification: No Action Indicated (NAI), source: FDA, date: January 25, 2019
- [FDA Inspection 1077108 - Kindeva Drug Delivery LP - 2019-01-25](https://www.keypedia.com/records/fda_inspections/kindeva-drug-delivery-lp/6c5c7b7a-2d7b-4a19-b560-de5ed4b35b3e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 25, 2019
- [FDA Inspection 1008836 - Kindeva Drug Delivery LP - 2017-03-06](https://www.keypedia.com/records/fda_inspections/kindeva-drug-delivery-lp/8b089b62-0981-4b0e-b0a0-a1ee934ee36c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 6, 2017
- [FDA Inspection 940328 - Kindeva Drug Delivery LP - 2015-09-01](https://www.keypedia.com/records/fda_inspections/kindeva-drug-delivery-lp/a384e9d5-4399-4a70-b142-3a65a384f89d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 1, 2015
- [FDA Inspection 896244 - Kindeva Drug Delivery LP - 2014-09-17](https://www.keypedia.com/records/fda_inspections/kindeva-drug-delivery-lp/54de6a46-22fb-4601-843a-8e1bc171c117) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 17, 2014
- [FDA Inspection 845595 - Kindeva Drug Delivery LP - 2013-08-23](https://www.keypedia.com/records/fda_inspections/kindeva-drug-delivery-lp/7408fcb9-1cbb-4ee6-ba35-3b28011ff325) — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2013
- [FDA Inspection 761084 - Kindeva Drug Delivery LP - 2012-01-04](https://www.keypedia.com/records/fda_inspections/kindeva-drug-delivery-lp/b83fe457-2719-4bc6-966a-6918d5d1d54b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 4, 2012
- [FDA Inspection 702983 - Kindeva Drug Delivery LP - 2010-11-05](https://www.keypedia.com/records/fda_inspections/kindeva-drug-delivery-lp/aa0df03c-6428-483b-b868-46fdb53fc99b) — classification: No Action Indicated (NAI), source: FDA, date: November 5, 2010

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