# FDA Inspection 1099820 - PerkinElmer Health Sciences, Inc. - August 01, 2019

Source: https://www.keypedia.com/records/fda_inspections/perkinelmer-health-sciences-inc/c27f58f2-9dc9-424d-b3da-e8ad19f2fd8f
Source feed: FDA_Inspections

> FDA Inspection 1099820 for PerkinElmer Health Sciences, Inc. on August 01, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099820
- Company Name: PerkinElmer Health Sciences, Inc.
- Inspection Date: 2019-08-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1049697 - 2018-04-05](https://www.keypedia.com/records/fda_inspections/perkinelmer-health-sciences-inc/58abcde8-fe21-413e-87c5-d2611361cc7b)
- [FDA Inspection 796603 - 2012-08-23](https://www.keypedia.com/records/fda_inspections/perkinelmer-health-sciences-inc/7efdf8f9-de48-4655-a294-5f9f6db31661)

Company: https://www.keypedia.com/companies/perkinelmer-health-sciences-inc/4442f82f-ae03-46cc-91cf-730a701af520

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7