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Clinical Controls Division FDA Record

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

No warning letters matched by name

Inspections 0 0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 1 Latest Aug 30, 2001

Clinical Controls Division has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Clinical Controls Division" is on file.

What these totals cover: FDA records filed under the name "Clinical Controls Division".

Latest 510(k): Aug 30, 2001

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	0	Nov 15, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

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Recent 510(k) clearances

1 510(k) clearance on Aug 30, 2001.

K-Number	Device	Date
K012855	LIQUISPX LIQUID LIPID CONTROL	Aug 30, 2001

Clinical Controls Division and the FDA: common questions

Has Clinical Controls Division received an FDA warning letter?

No FDA warning letter addressed to the name "Clinical Controls Division" 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 Clinical Controls Division received an FDA Form 483?

FDA has not published a Form 483 for "Clinical Controls Division" in its reading room. FDA publishes some Form 483s, not all of them.

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