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A. R. Hinkel Company, Inc. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Latest inspection NAI · Jan 13, 2023
No warning letters matched by name

Inspections 5

0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 1 Latest Oct 4, 1990

A. R. Hinkel Company, Inc. has 0 FDA recalls, 5 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "A. R. Hinkel Company, Inc." is on file.

What these totals cover: FDA records filed under the name "A. R. Hinkel Company, Inc." and its spelling variants "A. R. Hinkel Company", "A.R. Hinkel Co".

Latest inspection: Jan 13, 2023 · NAI
Latest 510(k): Oct 4, 1990

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 11, 2026 (checked Nov 15, 2026, unchanged)	File dated Nov 10, 2026	Current
510(k) clearances	1	Nov 15, 2026	File dated Nov 9, 2026	Current
Inspections	5	Nov 15, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

A. R. Hinkel Company, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

A. R. Hinkel Company, Inc.: FDA inspections per year

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	0	0	0	0	0
2024	0	0	0	0	0
2023	1	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	1	0	0	0	0
2019	0	0	0	0	0
2018	0	0	0	0	0
2017	0	0	0	0	0

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

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Recent FDA inspections

5 inspections from Oct 27, 2010 to Jan 13, 2023.

Date	Site	Product	Classification	FEI
Jan 13, 2023	Simi Valley, CA	Devices	No Action Indicated (NAI)	2020999
Jan 24, 2020	Simi Valley, CA	Devices	Voluntary Action Indicated (VAI)	2020999
Jun 6, 2016	Simi Valley, CA	Devices	Voluntary Action Indicated (VAI)	2020999
Oct 18, 2012	Simi Valley, CA	Devices	No Action Indicated (NAI)	2020999
Oct 27, 2010	Simi Valley, CA	Devices	No Action Indicated (NAI)	2020999

NAI: No objectionable conditions or practices were found during the inspection.
VAI: Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI: Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 2020999	Simi Valley, CA	5	Jan 13, 2023

Recent 510(k) clearances

1 510(k) clearance on Oct 4, 1990.

K-Number	Device	Date
K904015	ELECTRO-BLEND EPILATOR, MODEL UC-3	Oct 4, 1990

A. R. Hinkel Company, Inc. and the FDA: common questions

Has A. R. Hinkel Company, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "A. R. Hinkel Company, Inc." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has A. R. Hinkel Company, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "A. R. Hinkel Company, Inc." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect A. R. Hinkel Company, Inc.?

The most recent FDA inspection on file ended Jan 13, 2023 at Simi Valley, CA and was classified NAI. FDA has 5 inspections of A. R. Hinkel Company, Inc. on file.

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