# Antelope Valley Hospital a facility of Antelope Valley Hospital District, Lancaster, CA – FDA Inspections

Source: https://www.keypedia.com/companies/antelope-valley-hospital-a-facility-of-antelope-valley-hospital-district/cbb1cc22-5b12-4c72-95e0-cda8abaaa52a

> Inspection records and compliance data for Antelope Valley Hospital a facility of Antelope Valley Hospital District in Lancaster, California. 5 FDA inspections on record, last inspected February 27, 2020.

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## Details

- Name: Antelope Valley Hospital a facility of Antelope Valley Hospital District
- FEI Number: 2074565
- Address Line 1: 1600 W Avenue J
- City: Lancaster
- State: California
- Zip Code: 93534
- Country Name: United States
- Address: 1600 W Avenue J, Lancaster, California 93534, United States
- Country: United States

## Related Documents

- FDA Inspection 1121323 - Antelope Valley Hospital a facility of Antelope Valley Hospital District - 2020-02-27 — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2020
- FDA Inspection 1121323 - Antelope Valley Hospital a facility of Antelope Valley Hospital District - 2020-02-27 — classification: No Action Indicated (NAI), source: FDA, date: February 27, 2020
- FDA Inspection 1037069 - Antelope Valley Hospital a facility of Antelope Valley Hospital District - 2017-12-15 — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2017
- FDA Inspection 884272 - Antelope Valley Hospital a facility of Antelope Valley Hospital District - 2014-06-02 — classification: No Action Indicated (NAI), source: FDA, date: June 2, 2014
- [FDA Inspection 754236 - Antelope Valley Hospital a facility of Antelope Valley Hospital District - 2011-11-09](https://www.keypedia.com/records/fda_inspections/antelope-valley-hospital-a-facility-of-antelope-valley-hospital-district/d1d374ec-8fbd-4ee1-9fbc-f0ca472b22e5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 9, 2011
- FDA Inspection 644683 - Antelope Valley Hospital a facility of Antelope Valley Hospital District - 2010-02-05 — classification: No Action Indicated (NAI), source: FDA, date: February 5, 2010

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