# Sklar Instruments – FDA Inspection, Sep 30, 2011

Source: https://www.keypedia.com/records/fda_inspections/sklar-instruments/0b362f0e-0797-4fe3-be9a-8bb107320777
Source feed: FDA_Inspections

> FDA inspection 747975 of Sklar Instruments, September 30, 2011. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 747975
- Company Name: Sklar Instruments
- Inspection Date: 2011-09-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1105796 - 2018-11-09](https://www.keypedia.com/records/fda_inspections/sklar-instruments/4873ac1a-22b9-46b0-9e85-f8f9b81f44ae)
- [FDA Inspection 936721 - 2015-08-03](https://www.keypedia.com/records/fda_inspections/sklar-instruments/601f600c-27bc-40d2-8fe4-849db5e82625)

Company: https://www.keypedia.com/companies/sklar-instruments/8afc7560-be77-4f92-aa4b-daedabfd5c1b

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